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rs121908652

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908652(C;T)
Make rs121908652(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position22129682
GeneWNT4
is asnp
is mentioned by
dbSNPrs121908652
ebirs121908652
HLIrs121908652
Exacrs121908652
Varsomers121908652
Maprs121908652
PheGenIrs121908652
hapmaprs121908652
1000 genomesrs121908652
hgdprs121908652
ensemblrs121908652
gopubmedrs121908652
geneviewrs121908652
scholarrs121908652
googlers121908652
pharmgkbrs121908652
gwascentralrs121908652
openSNPrs121908652
23andMers121908652
23andMe allrs121908652
SNP Nexus

SNPshotrs121908652
SNPdbers121908652
MSV3drs121908652
GWAS Ctlgrs121908652
Max Magnitude0
OMIM603490
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121908652(T;T)
Alt rs121908652(T;T)
Reference rs121908652(C;C)
Significance Pathogenic
Disease Mullerian aplasia and hyperandrogenism
Variation info
Gene WNT4
CLNDBN Mullerian aplasia and hyperandrogenism
Reversed 1
HGVS NC_000001.10:g.22456175G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006690.2,