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rs779326570

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs779326570(C;T)
Make rs779326570(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position48968025
GeneWNT10B
is asnp
is mentioned by
dbSNPrs779326570
ebirs779326570
HLIrs779326570
Exacrs779326570
Varsomers779326570
Maprs779326570
PheGenIrs779326570
hapmaprs779326570
1000 genomesrs779326570
hgdprs779326570
ensemblrs779326570
gopubmedrs779326570
geneviewrs779326570
scholarrs779326570
googlers779326570
pharmgkbrs779326570
gwascentralrs779326570
openSNPrs779326570
23andMers779326570
23andMe allrs779326570
SNP Nexus

SNPshotrs779326570
SNPdbers779326570
MSV3drs779326570
GWAS Ctlgrs779326570
Max Magnitude0
ClinVar
Risk rs779326570(T;T)
Alt rs779326570(T;T)
Reference rs779326570(C;C)
Significance Pathogenic
Disease Tooth agenesis
Variation info
Gene WNT10B
CLNDBN Tooth agenesis, selective, 8
Reversed 0
HGVS NC_000012.11:g.49361808C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000239578.1,