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rs766021478

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs766021478(C;T)
Make rs766021478(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position48966479
GeneWNT10B
is asnp
is mentioned by
dbSNPrs766021478
ClinGenrs766021478
ebirs766021478
HLIrs766021478
Exacrs766021478
Varsomers766021478
Maprs766021478
PheGenIrs766021478
hapmaprs766021478
1000 genomesrs766021478
hgdprs766021478
ensemblrs766021478
gopubmedrs766021478
geneviewrs766021478
scholarrs766021478
googlers766021478
pharmgkbrs766021478
gwascentralrs766021478
openSNPrs766021478
23andMers766021478
23andMe allrs766021478
SNP Nexus

SNPshotrs766021478
SNPdbers766021478
MSV3drs766021478
GWAS Ctlgrs766021478
Max Magnitude0
ClinVar
Risk rs766021478(T;T)
Alt rs766021478(T;T)
Reference Rs766021478(C;C)
Significance Pathogenic
Disease Tooth agenesis
Variation info
Gene WNT10B
CLNDBN Tooth agenesis, selective, 8
Reversed 0
HGVS NC_000012.11:g.49360262C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000239472.1,