Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1554888939
rs1554888939
EHMT1
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1555738475
rs1555738475
STK11
T 0.700 CausalMutation CLINVAR

dbSNP: rs6259
rs6259
SHBG
0.010 GeneticVariation BEFREE Association of rs6259 polymorphism with SHBG levels and Poly Cystic Ovary Syndrome in Indian population: a case control study. 30719605

2019