Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121908650
rs121908650
WNT4
0.800 GeneticVariation UNIPROT Identification and functional analysis of a new WNT4 gene mutation among 28 adolescent girls with primary amenorrhea and müllerian duct abnormalities: a French collaborative study. 18182450

2008
dbSNP: rs121908653
rs121908653
WNT4 ; LOC105376845
0.800 GeneticVariation UNIPROT Identification and functional analysis of a new WNT4 gene mutation among 28 adolescent girls with primary amenorrhea and müllerian duct abnormalities: a French collaborative study. 18182450

2008
dbSNP: rs121908650
rs121908650
WNT4
0.800 GeneticVariation UNIPROT WNT4 deficiency--a clinical phenotype distinct from the classic Mayer-Rokitansky-Kuster-Hauser syndrome: a case report. 16959810

2007
dbSNP: rs121908653
rs121908653
WNT4 ; LOC105376845
0.800 GeneticVariation UNIPROT WNT4 deficiency--a clinical phenotype distinct from the classic Mayer-Rokitansky-Kuster-Hauser syndrome: a case report. 16959810

2007
dbSNP: rs121908650
rs121908650
WNT4
0.800 GeneticVariation UNIPROT A WNT4 mutation associated with Müllerian-duct regression and virilization in a 46,XX woman. 15317892

2004
dbSNP: rs121908653
rs121908653
WNT4 ; LOC105376845
0.800 GeneticVariation UNIPROT A WNT4 mutation associated with Müllerian-duct regression and virilization in a 46,XX woman. 15317892

2004
dbSNP: rs121908650
rs121908650
WNT4
C 0.800 CausalMutation CLINVAR

dbSNP: rs121908653
rs121908653
WNT4 ; LOC105376845
G 0.800 CausalMutation CLINVAR

dbSNP: rs121908652
rs121908652
WNT4
A 0.700 CausalMutation CLINVAR