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rs121908650

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121908650(A;G)
Make rs121908650(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position22120459
GeneWNT4
is asnp
is mentioned by
dbSNPrs121908650
ebirs121908650
HLIrs121908650
Exacrs121908650
Varsomers121908650
Maprs121908650
PheGenIrs121908650
hapmaprs121908650
1000 genomesrs121908650
hgdprs121908650
ensemblrs121908650
gopubmedrs121908650
geneviewrs121908650
scholarrs121908650
googlers121908650
pharmgkbrs121908650
gwascentralrs121908650
openSNPrs121908650
23andMers121908650
23andMe allrs121908650
SNP Nexus

SNPshotrs121908650
SNPdbers121908650
MSV3drs121908650
GWAS Ctlgrs121908650
Max Magnitude0
OMIM603490
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121908650(G;G)
Alt rs121908650(G;G)
Reference rs121908650(A;A)
Significance Pathogenic
Disease Mullerian aplasia and hyperandrogenism
Variation info
Gene WNT4
CLNDBN Mullerian aplasia and hyperandrogenism
Reversed 1
HGVS NC_000001.10:g.22446952T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000006688.2,