Have questions? Visit https://www.reddit.com/r/SNPedia

rs146902156

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 3 Likely miscall if from Ancestry data; otherwise, tooth agenesis mutation
(G;G) 0 common in clinvar
Make rs146902156(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position218890256
GeneWNT10A
is asnp
is mentioned by
dbSNPrs146902156
ClinGenrs146902156
ebirs146902156
HLIrs146902156
Exacrs146902156
Varsomers146902156
Maprs146902156
PheGenIrs146902156
hapmaprs146902156
1000 genomesrs146902156
hgdprs146902156
ensemblrs146902156
gopubmedrs146902156
geneviewrs146902156
scholarrs146902156
googlers146902156
pharmgkbrs146902156
gwascentralrs146902156
openSNPrs146902156
23andMers146902156
23andMe allrs146902156
SNP Nexus

SNPshotrs146902156
SNPdbers146902156
MSV3drs146902156
GWAS Ctlgrs146902156
Max Magnitude3
ClinVar
Risk Rs146902156(A;A)
Alt Rs146902156(A;A)
Reference Rs146902156(G;G)
Significance Pathogenic
Disease Tooth agenesis not provided Schopf-Schulz-Passarge syndrome Odontoonychodermal dysplasia Selective tooth agenesis
Variation info
Gene WNT10A
CLNDBN Tooth agenesis, selective, 4 not provided Schopf-Schulz-Passarge syndrome Odontoonychodermal dysplasia Selective tooth agenesis
Reversed 0
HGVS NC_000002.11:g.219754978G>A
CLNSRC OMIM Allelic Variant UniProtKB (protein) UniProtKB (variants)
CLNACC RCV000023530.3, RCV000059804.1, RCV000271824.1, RCV000322248.1, RCV000385003.1,


[PMID 21484994] WNT10A and isolated hypodontia.