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rs28933373

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs28933373(A;G)
Make rs28933373(G;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position36663163
GeneLOC105370455, PAX9
is asnp
is mentioned by
dbSNPrs28933373
dbSNP (classic)rs28933373
ClinGenrs28933373
ebirs28933373
HLIrs28933373
Exacrs28933373
Gnomadrs28933373
Varsomers28933373
LitVarrs28933373
Maprs28933373
PheGenIrs28933373
Biobankrs28933373
1000 genomesrs28933373
hgdprs28933373
ensemblrs28933373
geneviewrs28933373
scholarrs28933373
googlers28933373
pharmgkbrs28933373
gwascentralrs28933373
openSNPrs28933373
23andMers28933373
SNPshotrs28933373
SNPdbers28933373
MSV3drs28933373
GWAS Ctlgrs28933373
Max Magnitude0
OMIM167416
DescTOOTH AGENESIS, SELECTIVE, 3
Variant0004
Relatedalso


ClinVar
Risk rs28933373(G;G)
Alt rs28933373(G;G)
Reference Rs28933373(A;A)
Significance Pathogenic
Disease Tooth agenesis
Variation info
Gene PAX9
CLNDBN Tooth agenesis, selective, 3
Reversed 0
HGVS NC_000014.8:g.37132368A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000014780.26,