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rs121908119

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908119(A;A)
Make rs121908119(A;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position218882368
GeneWNT10A
is asnp
is mentioned by
dbSNPrs121908119
ebirs121908119
HLIrs121908119
Exacrs121908119
Varsomers121908119
Maprs121908119
PheGenIrs121908119
hapmaprs121908119
1000 genomesrs121908119
hgdprs121908119
ensemblrs121908119
gopubmedrs121908119
geneviewrs121908119
scholarrs121908119
googlers121908119
pharmgkbrs121908119
gwascentralrs121908119
openSNPrs121908119
23andMers121908119
23andMe allrs121908119
SNP Nexus

SNPshotrs121908119
SNPdbers121908119
MSV3drs121908119
GWAS Ctlgrs121908119
Max Magnitude0
OMIM606268
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121908119(A;A)
Alt rs121908119(A;A)
Reference rs121908119(C;C)
Significance Pathogenic
Disease Odontoonychodermal dysplasia Schopf-Schulz-Passarge syndrome Tooth agenesis Inborn genetic diseases
Variation info
Gene WNT10A
CLNDBN Odontoonychodermal dysplasia Schopf-Schulz-Passarge syndrome Tooth agenesis, selective, 4 Inborn genetic diseases
Reversed 0
HGVS NC_000002.11:g.219747090C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000004715.3, RCV000004716.3, RCV000030650.3, RCV000190800.1,