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rs28933972

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs28933972(C;T)
Make rs28933972(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position36662968
GenePAX9
is asnp
is mentioned by
dbSNPrs28933972
ebirs28933972
HLIrs28933972
Exacrs28933972
Varsomers28933972
Maprs28933972
PheGenIrs28933972
hapmaprs28933972
1000 genomesrs28933972
hgdprs28933972
ensemblrs28933972
gopubmedrs28933972
geneviewrs28933972
scholarrs28933972
googlers28933972
pharmgkbrs28933972
gwascentralrs28933972
openSNPrs28933972
23andMers28933972
23andMe allrs28933972
SNP Nexus

SNPshotrs28933972
SNPdbers28933972
MSV3drs28933972
GWAS Ctlgrs28933972
Max Magnitude0
OMIM167416
DescTOOTH AGENESIS, SELECTIVE, 3
Variant0008
Relatedalso
Neighborrs28933970
Distance14
Neighborrs28933971
Distance7


ClinVar
Risk rs28933972(T;T)
Alt rs28933972(T;T)
Reference rs28933972(C;C)
Significance Pathogenic
Disease Tooth agenesis
Variation info
Gene PAX9
CLNDBN Tooth agenesis, selective, 3
Reversed 0
HGVS NC_000014.8:g.37132173C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000014784.22,