Rs104894468

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Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs104894468(A;T)
Make rs104894468(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position36663151
GenePAX9
is asnp
is mentioned by
dbSNPrs104894468
Exacrs104894468
PheGenIrs104894468
nextbiors104894468
hapmaprs104894468
1000 genomesrs104894468
hgdprs104894468
ensemblrs104894468
gopubmedrs104894468
geneviewrs104894468
scholarrs104894468
googlers104894468
pharmgkbrs104894468
gwascentralrs104894468
openSNPrs104894468
23andMers104894468
23andMe allrs104894468
SNP Nexus

SNPshotrs104894468
SNPdbers104894468
MSV3drs104894468
OMIM167416
Desc
Variant0009
Relatedalso
ClinVar
Risk rs104894468(T;T)
Alt rs104894468(T;T)
Reference rs104894468(A;A)
Significance Pathogenic
Disease Tooth agenesis
Variation info
Gene PAX9
CLNDBN Tooth agenesis, selective, 3
Reversed 0
HGVS NC_000014.8:g.37132356A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000014785.23,