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rs28933970

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs28933970(C;C)
Make rs28933970(C;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position36662954
GenePAX9
is asnp
is mentioned by
dbSNPrs28933970
ebirs28933970
HLIrs28933970
Exacrs28933970
Varsomers28933970
Maprs28933970
PheGenIrs28933970
hapmaprs28933970
1000 genomesrs28933970
hgdprs28933970
ensemblrs28933970
gopubmedrs28933970
geneviewrs28933970
scholarrs28933970
googlers28933970
pharmgkbrs28933970
gwascentralrs28933970
openSNPrs28933970
23andMers28933970
23andMe allrs28933970
SNP Nexus

SNPshotrs28933970
SNPdbers28933970
MSV3drs28933970
GWAS Ctlgrs28933970
Max Magnitude0
OMIM167416
DescTOOTH AGENESIS, SELECTIVE, 3
Variant0005
Relatedalso
Neighborrs28933972
Distance14


ClinVar
Risk rs28933970(C;C)
Alt rs28933970(C;C)
Reference rs28933970(T;T)
Significance Pathogenic
Disease Tooth agenesis
Variation info
Gene PAX9
CLNDBN Tooth agenesis, selective, 3
Reversed 0
HGVS NC_000014.8:g.37132159T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000014781.25,