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rs121908121

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908121(A;A)
Make rs121908121(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position218889990
GeneWNT10A
is asnp
is mentioned by
dbSNPrs121908121
ebirs121908121
HLIrs121908121
Exacrs121908121
Varsomers121908121
Maprs121908121
PheGenIrs121908121
hapmaprs121908121
1000 genomesrs121908121
hgdprs121908121
ensemblrs121908121
gopubmedrs121908121
geneviewrs121908121
scholarrs121908121
googlers121908121
pharmgkbrs121908121
gwascentralrs121908121
openSNPrs121908121
23andMers121908121
23andMe allrs121908121
SNP Nexus

SNPshotrs121908121
SNPdbers121908121
MSV3drs121908121
GWAS Ctlgrs121908121
Max Magnitude0
OMIM606268
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121908121(A;A)
Alt rs121908121(A;A)
Reference rs121908121(G;G)
Significance Pathogenic
Disease Odontoonychodermal dysplasia Tooth agenesis not provided
Variation info
Gene WNT10A
CLNDBN Odontoonychodermal dysplasia Tooth agenesis, selective, 4 not provided
Reversed 0
HGVS NC_000002.11:g.219754712G>A
CLNSRC OMIM Allelic Variant UniProtKB (variants)
CLNACC RCV000004718.3, RCV000030651.3, RCV000059803.1,


[PMID 22581971] Mutations in WNT10A are present in more than half of isolated hypodontia cases.