Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2275558
rs2275558
PBX1
0.010 GeneticVariation BEFREE The dominant models of rs34072914 and rs2275558 in WNT9B and PBX1, respectively, were significantly associated with MRKH syndrome risk in the Chinese Han patients. 26075712

2015
dbSNP: rs34072914
rs34072914
WNT9B ; LRRC37A2
0.010 GeneticVariation BEFREE The dominant models of rs34072914 and rs2275558 in WNT9B and PBX1, respectively, were significantly associated with MRKH syndrome risk in the Chinese Han patients. 26075712

2015
dbSNP: rs2070074
rs2070074
GALT
0.010 GeneticVariation BEFREE Vaginal agenesis (Mayer-Rokitansky-Kuster-Hauser syndrome) associated with the N314D mutation of galactose-1-phosphate uridyl transferase (GALT). 9238673

1996