Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Genetic Drift	[NCBI]

Gene	Link	Information Gain
TRNL1	[NCBI]	0.000135654
USP26	[NCBI]	3.87001e-06
GRASP	[NCBI]	3.83748e-06
ERVWE1	[NCBI]	3.32723e-06
BSCL2	[NCBI]	3.26969e-06
RHD	[NCBI]	3.06903e-06
KRIT1	[NCBI]	2.99933e-06
RHCE	[NCBI]	2.95666e-06
HEXA	[NCBI]	2.95666e-06
ABO	[NCBI]	2.91352e-06
ERCC4	[NCBI]	2.77003e-06
ADH1B	[NCBI]	2.68291e-06
APEX1	[NCBI]	2.65879e-06
MSH3	[NCBI]	2.61195e-06
CYP2E1	[NCBI]	2.44242e-06
XRCC1	[NCBI]	2.32153e-06
ALDH2	[NCBI]	2.27791e-06
ERCC2	[NCBI]	2.24279e-06
HP	[NCBI]	2.21107e-06
HLA-DQB1	[NCBI]	1.96537e-06
CYP2C19	[NCBI]	1.93779e-06
G6PD	[NCBI]	1.8834e-06
APC	[NCBI]	1.85788e-06
ACE	[NCBI]	1.81047e-06
MLH1	[NCBI]	1.6897e-06

OMIM	Link	Information gain
TSD	[NCBI]	0.000262742
HSAN3	[NCBI]	0.000215513
canavan disease	[NCBI]	0.000107086
mucolipidosis iv	[NCBI]	0.000105132
niemann-pick disease, type a	[NCBI]	0.000104223
DFNB1	[NCBI]	0.000100951
cystinuria	[NCBI]	9.74962e-05
glycogen storage disease vii	[NCBI]	9.68716e-05
lactase persistence	[NCBI]	9.45527e-05
HHF1	[NCBI]	9.34872e-05
DYT1	[NCBI]	9.05954e-05
APC	[NCBI]	9.00429e-05
gaucher disease, type i	[NCBI]	8.41415e-05
BLM	[NCBI]	7.92801e-05
hypercholesterolemia, autosomal dominant	[NCBI]	7.37828e-05
leber optic atrophy	[NCBI]	6.2989e-05
MCM6	[NCBI]	4.05605e-05
pta deficiency	[NCBI]	3.55954e-05
ADH2	[NCBI]	3.53752e-05
ALDH2	[NCBI]	3.33754e-05
FANCC	[NCBI]	3.3223e-05
MTTL1	[NCBI]	2.89952e-05
HEXA	[NCBI]	2.81709e-05
BRCA2	[NCBI]	2.58645e-05
apc gene	[NCBI]	2.44108e-05
GJB2	[NCBI]	2.3861e-05
BRCA1	[NCBI]	2.26142e-05
SOD1	[NCBI]	2.16711e-05
CRC	[NCBI]	1.94393e-05
G6PD	[NCBI]	1.28969e-05
CF	[NCBI]	3.32939e-06