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rs121908122

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908122(A;A)
Make rs121908122(A;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position218893145
GeneWNT10A
is asnp
is mentioned by
dbSNPrs121908122
ebirs121908122
HLIrs121908122
Exacrs121908122
Varsomers121908122
Maprs121908122
PheGenIrs121908122
hapmaprs121908122
1000 genomesrs121908122
hgdprs121908122
ensemblrs121908122
gopubmedrs121908122
geneviewrs121908122
scholarrs121908122
googlers121908122
pharmgkbrs121908122
gwascentralrs121908122
openSNPrs121908122
23andMers121908122
23andMe allrs121908122
SNP Nexus

SNPshotrs121908122
SNPdbers121908122
MSV3drs121908122
GWAS Ctlgrs121908122
Max Magnitude0
OMIM606268
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121908122(A;A)
Alt rs121908122(A;A)
Reference rs121908122(C;C)
Significance Pathogenic
Disease Odontoonychodermal dysplasia
Variation info
Gene WNT10A
CLNDBN Odontoonychodermal dysplasia
Reversed 0
HGVS NC_000002.11:g.219757867C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000004719.2,