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rs121918349

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121918349(C;T)
Make rs121918349(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position48966271
GeneWNT10B
is asnp
is mentioned by
dbSNPrs121918349
ebirs121918349
HLIrs121918349
Exacrs121918349
Varsomers121918349
Maprs121918349
PheGenIrs121918349
hapmaprs121918349
1000 genomesrs121918349
hgdprs121918349
ensemblrs121918349
gopubmedrs121918349
geneviewrs121918349
scholarrs121918349
googlers121918349
pharmgkbrs121918349
gwascentralrs121918349
openSNPrs121918349
23andMers121918349
23andMe allrs121918349
SNP Nexus

SNPshotrs121918349
SNPdbers121918349
MSV3drs121918349
GWAS Ctlgrs121918349
Max Magnitude0
OMIM601906
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121918349(A,G,T;A,G,T)
Alt rs121918349(A,G,T;A,G,T)
Reference rs121918349(C;C)
Significance Pathogenic
Disease Split-hand/foot malformation 6
Variation info
Gene WNT10B
CLNDBN Split-hand/foot malformation 6
Reversed 1
HGVS NC_000012.11:g.49360054G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000008069.4,