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rs113993963

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs113993963(A;C)
Make rs113993963(C;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position189789816
GeneTP63
is asnp
is mentioned by
dbSNPrs113993963
ebirs113993963
HLIrs113993963
Exacrs113993963
Varsomers113993963
Maprs113993963
PheGenIrs113993963
hapmaprs113993963
1000 genomesrs113993963
hgdprs113993963
ensemblrs113993963
gopubmedrs113993963
geneviewrs113993963
scholarrs113993963
googlers113993963
pharmgkbrs113993963
gwascentralrs113993963
openSNPrs113993963
23andMers113993963
23andMe allrs113993963
SNP Nexus

SNPshotrs113993963
SNPdbers113993963
MSV3drs113993963
GWAS Ctlgrs113993963
Max Magnitude0
OMIM603273
Desc
Variant0011
Relatedalso
ClinVar
Risk rs113993963(C;C)
Alt rs113993963(C;C)
Reference rs113993963(A;A)
Significance Pathogenic
Disease ADULT syndrome
Variation info
Gene TP63
CLNDBN ADULT syndrome
Reversed 0
HGVS NC_000003.11:g.189507605A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000006911.2,