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

rs28933971

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs28933971(C;C)
Make rs28933971(C;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position36662975
GenePAX9
is asnp
is mentioned by
dbSNPrs28933971
ebirs28933971
HLIrs28933971
Exacrs28933971
Varsomers28933971
Maprs28933971
PheGenIrs28933971
hapmaprs28933971
1000 genomesrs28933971
hgdprs28933971
ensemblrs28933971
gopubmedrs28933971
geneviewrs28933971
scholarrs28933971
googlers28933971
pharmgkbrs28933971
gwascentralrs28933971
openSNPrs28933971
23andMers28933971
23andMe allrs28933971
SNP Nexus

SNPshotrs28933971
SNPdbers28933971
MSV3drs28933971
GWAS Ctlgrs28933971
Max Magnitude0
OMIM167416
DescTOOTH AGENESIS, SELECTIVE, 3
Variant0007
Relatedalso
Neighborrs28933972
Distance7
Neighborrs28933373
Distance188


ClinVar
Risk rs28933971(C;C)
Alt rs28933971(C;C)
Reference rs28933971(G;G)
Significance Pathogenic
Disease Tooth agenesis
Variation info
Gene PAX9
CLNDBN Tooth agenesis, selective, 3
Reversed 0
HGVS NC_000014.8:g.37132180G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000014783.25,