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01 Twins, Dizygotic [NCBI]

Gene


 Gene Link Information
Gain		 01
MS [NCBI] 0.000507905
BP36 [NCBI] 0.0001481
BP37 [NCBI] 0.0001481
MYAS1 [NCBI] 0.0001481
BP39 [NCBI] 0.0001481
BP38 [NCBI] 0.0001481
DFNA18 [NCBI] 0.000122826
VUR [NCBI] 8.98888e-05
WG [NCBI] 8.11797e-05
FOP [NCBI] 6.89289e-05
AIS [NCBI] 4.29807e-05
SLC6A4 [NCBI] 7.80771e-06
BMP15 [NCBI] 7.57681e-06
CYP2A6 [NCBI] 7.44518e-06
GDF9 [NCBI] 7.36759e-06
SHBG [NCBI] 7.09876e-06
APOB [NCBI] 6.57726e-06
LEP [NCBI] 5.40508e-06
SLC6A3 [NCBI] 5.18598e-06
FMR1 [NCBI] 4.77125e-06
MC1R [NCBI] 4.2402e-06
ADRB3 [NCBI] 4.1243e-06
CFTR [NCBI] 4.08185e-06
SNAP25 [NCBI] 4.05454e-06
LEPR [NCBI] 3.94784e-06
LPL [NCBI] 3.55716e-06
SRY [NCBI] 3.53159e-06
DRD4 [NCBI] 2.99703e-06
NOD2 [NCBI] 2.95062e-06
PPARG [NCBI] 2.91588e-06
MYOZ2 [NCBI] 2.87879e-06
RARS [NCBI] 2.82675e-06
SPG11 [NCBI] 2.80281e-06
GLS [NCBI] 2.78007e-06
KIAA0319 [NCBI] 2.71797e-06
TSNAX [NCBI] 2.66334e-06
GRK4 [NCBI] 2.66334e-06
BBS2 [NCBI] 2.66334e-06
TAS2R38 [NCBI] 2.63027e-06
PTH [NCBI] 2.57435e-06
KCNMB1 [NCBI] 2.57057e-06
BBS1 [NCBI] 2.57057e-06
GYS1 [NCBI] 2.57057e-06
ANKK1 [NCBI] 2.49359e-06
ATN1 [NCBI] 2.44868e-06
HSD3B1 [NCBI] 2.43811e-06
EPHX2 [NCBI] 2.40782e-06
GAD1 [NCBI] 2.40782e-06
ERCC8 [NCBI] 2.39816e-06
ALDH5A1 [NCBI] 2.37942e-06
GAD2 [NCBI] 2.3527e-06
KL [NCBI] 2.33573e-06
MTHFR [NCBI] 2.32879e-06
PTPRJ [NCBI] 2.29588e-06
CYP27B1 [NCBI] 2.28087e-06
RAD23B [NCBI] 2.27355e-06
CHRM2 [NCBI] 2.25227e-06
GLB1 [NCBI] 2.23862e-06
SLC26A2 [NCBI] 2.20619e-06
PRTN3 [NCBI] 2.20619e-06
SFTPB [NCBI] 2.17593e-06
ABCG8 [NCBI] 2.17593e-06
ABCG5 [NCBI] 2.16438e-06
AFP [NCBI] 2.10876e-06
MASP2 [NCBI] 2.10561e-06
CAPN10 [NCBI] 2.086e-06
ADIPOR2 [NCBI] 2.08123e-06
HRG [NCBI] 2.0765e-06
CYP2B6 [NCBI] 2.06721e-06
DRD5 [NCBI] 1.97965e-06
MPZ [NCBI] 1.96842e-06
ADIPOR1 [NCBI] 1.96109e-06
DISC1 [NCBI] 1.94326e-06
RPGR [NCBI] 1.94326e-06
ERCC6 [NCBI] 1.93289e-06
ADH1C [NCBI] 1.91613e-06
FANCC [NCBI] 1.91613e-06
F13A1 [NCBI] 1.85183e-06
TSHR [NCBI] 1.84057e-06
ADRB1 [NCBI] 1.83779e-06
PTPRN [NCBI] 1.7956e-06
XRCC3 [NCBI] 1.7956e-06
ADH1B [NCBI] 1.78564e-06
VWF [NCBI] 1.76895e-06
TSC2 [NCBI] 1.76637e-06
COMP [NCBI] 1.75935e-06
GNB3 [NCBI] 1.71517e-06
TYRP1 [NCBI] 1.71517e-06
CDKN1C [NCBI] 1.68666e-06
IGFBP1 [NCBI] 1.6769e-06
ATXN3 [NCBI] 1.66924e-06
CASR [NCBI] 1.64523e-06
XPC [NCBI] 1.64523e-06
HBA1 [NCBI] 1.62933e-06
ATXN1 [NCBI] 1.6276e-06
ABCA1 [NCBI] 1.61904e-06
APOE [NCBI] 1.61847e-06
XPA [NCBI] 1.5911e-06
HTR2A [NCBI] 1.58951e-06
PIK3R1 [NCBI] 1.55886e-06
IGFBP3 [NCBI] 1.52329e-06
MATN1 [NCBI] 1.49805e-06
MBL2 [NCBI] 1.49547e-06
APOA1 [NCBI] 1.49291e-06
DBH [NCBI] 1.4891e-06
SGK1 [NCBI] 1.4693e-06
NR3C1 [NCBI] 1.42776e-06
DRD2 [NCBI] 1.4212e-06
PMP22 [NCBI] 1.39081e-06
WAS [NCBI] 1.3898e-06
GATA1 [NCBI] 1.38478e-06
ADRB2 [NCBI] 1.35673e-06
ERCC2 [NCBI] 1.35022e-06
JAG1 [NCBI] 1.3429e-06
PKD1 [NCBI] 1.32861e-06
ADIPOQ [NCBI] 1.31733e-06
LDLR [NCBI] 1.31138e-06
PRL [NCBI] 1.31073e-06
INS [NCBI] 1.27031e-06
ERBB2 [NCBI] 1.26572e-06
GJB1 [NCBI] 1.21081e-06
IGF1 [NCBI] 1.20548e-06
GJB2 [NCBI] 1.11299e-06
PTPN11 [NCBI] 1.1009e-06
COMT [NCBI] 1.01619e-06
G6PD [NCBI] 9.9998e-07
HFE [NCBI] 9.18098e-07
IL6 [NCBI] 8.35992e-07
JAK2 [NCBI] 8.33541e-07
VDR [NCBI] 8.24947e-07
STAT3 [NCBI] 7.20128e-07
NOS3 [NCBI] 7.18708e-07
VEGFA [NCBI] 6.17371e-07
TGFB1 [NCBI] 6.02389e-07
BDNF [NCBI] 5.75273e-07
TH [NCBI] 5.71445e-07
EPO [NCBI] 5.64978e-07
ACHE [NCBI] 5.36282e-07
NPY [NCBI] 4.67104e-07



OMIM


 OMIM Link Information
gain		 01
twinning, dizygotic [NCBI] 0.00830336
autism [NCBI] 0.00229638
MENOQ1 [NCBI] 0.00119001
ANON1 [NCBI] 0.00113159
theophylline biotransformation [NCBI] 0.000990729
mammographic density [NCBI] 0.000990729
bone size quantitative trait locus 1 [NCBI] 0.000627545
renal-hepatic-pancreatic dysplasia with dandy-walker cyst [NCBI] 0.000627545
tune deafness [NCBI] 0.000627545
astigmatism [NCBI] 0.000627545
DYX6 [NCBI] 0.000563606
MAFD2 [NCBI] 0.000553856
jejunal atresia [NCBI] 0.000478883
MNG1 [NCBI] 0.000447918
centralopathic epilepsy [NCBI] 0.000378425
BULN1 [NCBI] 0.000378425
telomere length, mean leukocyte [NCBI] 0.000343986
PAND1 [NCBI] 0.000302828
alopecia areata 1 [NCBI] 0.000302828
aneurysm, intracranial berry, 1 [NCBI] 0.000260489
RA [NCBI] 0.000254008
vitamin d-dependent rickets, type ii [NCBI] 0.000244495
holoprosencephaly [NCBI] 0.000188521
DYX1 [NCBI] 0.000185543
DWS [NCBI] 0.000182996
PCD [NCBI] 0.000182996
twinning, monozygotic [NCBI] 0.000163424
MS [NCBI] 0.000154187
PCOS1 [NCBI] 0.000149771
GBD1 [NCBI] 0.000147199
BMND1 [NCBI] 0.000135761
HMS1 [NCBI] 0.000129655
FSHR [NCBI] 0.000127701
DYX2 [NCBI] 0.00012438
nasal alar collapse, bilateral [NCBI] 0.000123493
ureterocele [NCBI] 0.000123493
folate level in erythrocytes [NCBI] 0.000123493
lip prints [NCBI] 0.000123493
twinning due to superfetation [NCBI] 0.000123493
jejunal atresia with renal adysplasia [NCBI] 0.000123493
PPAB [NCBI] 0.000123493
breast cancer [NCBI] 0.000123089
ETM1 [NCBI] 0.000115597
CPI [NCBI] 0.000112999
osteoporosis [NCBI] 0.000110118
ADHD [NCBI] 0.000105526
OFC1 [NCBI] 9.74242e-05
lithium transport [NCBI] 9.57611e-05
acne, adult [NCBI] 9.57611e-05
langerhans cell histiocytosis [NCBI] 9.57611e-05
periodontitis, chronic [NCBI] 9.57611e-05
craniostenosis, sagittal, with congenital heart disease, mental deficiency, and mandibular ankylosis [NCBI] 9.57611e-05
EIG [NCBI] 8.85437e-05
RTS [NCBI] 8.67743e-05
androstenone, ability to smell [NCBI] 8.53201e-05
aprosencephaly syndrome [NCBI] 8.53201e-05
hydroxyprolinemia [NCBI] 7.85544e-05
fecundity gene, booroola, of sheep, homolog of [NCBI] 7.85544e-05
EEG [NCBI] 7.85544e-05
hair whorl [NCBI] 7.85544e-05
atrioventricular conduction time [NCBI] 7.85544e-05
respiratory underresponsiveness to hypoxia and hypercapnia [NCBI] 7.85544e-05
hand clasping pattern [NCBI] 7.85544e-05
tongue curling, folding, or rolling [NCBI] 7.85544e-05
oculocerebrocutaneous syndrome [NCBI] 7.35343e-05
lichen planus, familial [NCBI] 7.35343e-05
respiratory distress syndrome in premature infants [NCBI] 7.35343e-05
MDD [NCBI] 7.28183e-05
nasopharyngeal carcinoma [NCBI] 6.95422e-05
whistling face syndrome, recessive form [NCBI] 6.95422e-05
EHBA [NCBI] 6.95422e-05
HPE4 [NCBI] 6.95422e-05
creatine phosphokinase, elevated serum [NCBI] 6.95422e-05
EPHX2 [NCBI] 6.47747e-05
vacterl association with hydrocephalus, x-linked [NCBI] 6.33997e-05
IDD [NCBI] 6.33997e-05
SLE [NCBI] 6.14927e-05
OCA3 [NCBI] 6.09309e-05
EDM4 [NCBI] 6.09309e-05
tobacco addiction, susceptibility to [NCBI] 6.09309e-05
aryl hydrocarbon hydroxylase inducibility [NCBI] 5.87423e-05
hematopoietic stem cell kinetics, control of [NCBI] 5.87423e-05
SLC26A2 [NCBI] 5.79263e-05
DA2B [NCBI] 5.49957e-05
HPE2 [NCBI] 5.49957e-05
hypercholesterolemia, autosomal dominant [NCBI] 5.33776e-05
SHEP1 [NCBI] 5.33663e-05
parkinson disease, mitochondrial [NCBI] 5.33663e-05
HSR [NCBI] 5.31141e-05
SCZD9 [NCBI] 5.18657e-05
COFS1 [NCBI] 5.18657e-05
CYP1A1 [NCBI] 5.07606e-05
UMS [NCBI] 5.04755e-05
aging [NCBI] 5.04755e-05
hypophosphatasia, adult type [NCBI] 5.04755e-05
HPE3 [NCBI] 5.04755e-05
helicobacter pylori infection, susceptibility to [NCBI] 4.91809e-05
longevity [NCBI] 4.797e-05
BFLS [NCBI] 4.57613e-05
stroke, ischemic [NCBI] 4.47485e-05
APL [NCBI] 4.37884e-05
PI [NCBI] 4.29669e-05
CHNG2 [NCBI] 4.20072e-05
hodgkin lymphoma [NCBI] 4.20072e-05
diastrophic dysplasia [NCBI] 4.20072e-05
sudden infant death syndrome [NCBI] 4.20072e-05
osteoarthritis [NCBI] 3.96254e-05
lung cancer [NCBI] 3.96254e-05
CF [NCBI] 3.82825e-05
SPDA1 [NCBI] 3.81966e-05
HSAS [NCBI] 3.81966e-05
mycobacterium tuberculosis, susceptibility to [NCBI] 3.7523e-05
hypophosphatasia, infantile [NCBI] 3.68741e-05
MYOZ2 [NCBI] 3.58735e-05
SGBS1 [NCBI] 3.56439e-05
TSNAX [NCBI] 3.3854e-05
GCPS [NCBI] 3.3417e-05
malaria, susceptibility to [NCBI] 3.3417e-05
nijmegen breakage syndrome [NCBI] 3.29024e-05
GDF9 [NCBI] 3.23529e-05
GLS [NCBI] 3.23529e-05
POAG [NCBI] 3.14461e-05
FOP [NCBI] 3.14461e-05
PLA2G1B [NCBI] 3.1157e-05
P2RX4 [NCBI] 3.1157e-05
IGER [NCBI] 3.09872e-05
VDR [NCBI] 2.95834e-05
obesity [NCBI] 2.77123e-05
SULT1A1 [NCBI] 2.62808e-05
SFTPD [NCBI] 2.62808e-05
FSHB [NCBI] 2.54016e-05
MKS1 [NCBI] 2.499e-05
CYP1A2 [NCBI] 2.46368e-05
CES [NCBI] 2.40798e-05
SHBG [NCBI] 2.3657e-05
TD1 [NCBI] 2.35016e-05
CHH [NCBI] 2.35016e-05
ERCC6 [NCBI] 2.33536e-05
SLC25A20 [NCBI] 2.23014e-05
ALDH1A1 [NCBI] 2.16204e-05
DISC1 [NCBI] 2.10106e-05
fructose intolerance, hereditary [NCBI] 2.0637e-05
ALPL [NCBI] 2.0637e-05
PTPN11 [NCBI] 2.0637e-05
MTTK [NCBI] 2.0118e-05
TYRP1 [NCBI] 1.99548e-05
NDP [NCBI] 1.97961e-05
NS1 [NCBI] 1.97603e-05
ALDH2 [NCBI] 1.96416e-05
JAG1 [NCBI] 1.94912e-05
ABO [NCBI] 1.94912e-05
ADIPOQ [NCBI] 1.87926e-05
FLNA [NCBI] 1.76076e-05
AD [NCBI] 1.75896e-05
cortisol 11-beta-ketoreductase deficiency [NCBI] 1.67173e-05
hla-d histocompatibility type [NCBI] 1.64484e-05
TGFB1 [NCBI] 1.63623e-05
TSC2 [NCBI] 1.58683e-05
SCZD [NCBI] 1.5304e-05
HRG [NCBI] 1.52001e-05
MTHFR [NCBI] 1.50618e-05
ichthyosis, x-linked [NCBI] 1.45405e-05
mucopolysaccharidosis type ii [NCBI] 1.45405e-05
MPZ [NCBI] 1.43569e-05
GH1 [NCBI] 1.39509e-05
SRY [NCBI] 1.38401e-05
ACH [NCBI] 1.38247e-05
MC1R [NCBI] 1.36251e-05
BBS [NCBI] 1.30181e-05
PKD1 [NCBI] 1.28864e-05
GJB1 [NCBI] 1.28864e-05
PCD [NCBI] 1.23868e-05
LPL [NCBI] 1.21628e-05
APOB [NCBI] 1.17827e-05
LEP [NCBI] 1.14054e-05
CASR [NCBI] 1.1336e-05
COMP [NCBI] 9.84556e-06
MG [NCBI] 8.65564e-06
fragile x mental retardation syndrome [NCBI] 8.53603e-06
FMF [NCBI] 8.38647e-06
WBS [NCBI] 8.28915e-06
MBL2 [NCBI] 7.4041e-06
INS [NCBI] 7.38845e-06
VEGF [NCBI] 6.79482e-06
ACE [NCBI] 5.61998e-06
AFP [NCBI] 3.71888e-06
WAS [NCBI] 2.69957e-06
BWS [NCBI] 2.54099e-06
GTS [NCBI] 1.53917e-06
G6PD [NCBI] 1.49297e-06
polycystic kidneys [NCBI] 1.32852e-06
ALD [NCBI] 1.19272e-06
PD [NCBI] 8.8748e-07
RP [NCBI] 8.33089e-07
NPY [NCBI] 6.3339e-07
CFTR [NCBI] 3.77719e-07
FA [NCBI] 3.19354e-07
PTH [NCBI] 2.05118e-07
ACHE [NCBI] 1.86987e-07
TH [NCBI] 1.517e-07
TS [NCBI] 1.46289e-07
PRL [NCBI] 9.33713e-08
APOE [NCBI] 7.57413e-08
EPO [NCBI] 3.08642e-08
CEACAM5 [NCBI] 2.4167e-09
FTD [NCBI] 1.74349e-09
BDNF [NCBI] 1.36242e-09
IS1 [NCBI] 4.4402e-10



Database Center for Life Science