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rs121908651

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908651(C;T)
Make rs121908651(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position22121549
GeneWNT4
is asnp
is mentioned by
dbSNPrs121908651
ebirs121908651
HLIrs121908651
Exacrs121908651
Varsomers121908651
Maprs121908651
PheGenIrs121908651
hapmaprs121908651
1000 genomesrs121908651
hgdprs121908651
ensemblrs121908651
gopubmedrs121908651
geneviewrs121908651
scholarrs121908651
googlers121908651
pharmgkbrs121908651
gwascentralrs121908651
openSNPrs121908651
23andMers121908651
23andMe allrs121908651
SNP Nexus

SNPshotrs121908651
SNPdbers121908651
MSV3drs121908651
GWAS Ctlgrs121908651
Max Magnitude0
OMIM603490
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121908651(T;T)
Alt rs121908651(T;T)
Reference rs121908651(C;C)
Significance Pathogenic
Disease Serkal syndrome
Variation info
Gene WNT4
CLNDBN Serkal syndrome
Reversed 1
HGVS NC_000001.10:g.22448042G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006689.2,