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rs147680216

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs147680216(A;A)
Make rs147680216(A;G)
ReferenceGRCh38 38.1/142
Chromosome2
Position218890244
GeneWNT10A
is asnp
is mentioned by
dbSNPrs147680216
ebirs147680216
HLIrs147680216
Exacrs147680216
Varsomers147680216
Maprs147680216
PheGenIrs147680216
hapmaprs147680216
1000 genomesrs147680216
hgdprs147680216
ensemblrs147680216
gopubmedrs147680216
geneviewrs147680216
scholarrs147680216
googlers147680216
pharmgkbrs147680216
gwascentralrs147680216
openSNPrs147680216
23andMers147680216
23andMe allrs147680216
SNP Nexus

SNPshotrs147680216
SNPdbers147680216
MSV3drs147680216
GWAS Ctlgrs147680216
Max Magnitude0
ClinVar
Risk rs147680216(A;A)
Alt rs147680216(A;A)
Reference rs147680216(G;G)
Significance Pathogenic
Disease Tooth agenesis
Variation info
Gene WNT10A
CLNDBN Tooth agenesis, selective, 4
Reversed 0
HGVS NC_000002.11:g.219754966G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000128463.2,