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rs113993965

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs113993965(A;A)
Make rs113993965(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position189808465
GeneTP63
is asnp
is mentioned by
dbSNPrs113993965
ebirs113993965
HLIrs113993965
Exacrs113993965
Varsomers113993965
Maprs113993965
PheGenIrs113993965
hapmaprs113993965
1000 genomesrs113993965
hgdprs113993965
ensemblrs113993965
gopubmedrs113993965
geneviewrs113993965
scholarrs113993965
googlers113993965
pharmgkbrs113993965
gwascentralrs113993965
openSNPrs113993965
23andMers113993965
23andMe allrs113993965
SNP Nexus

SNPshotrs113993965
SNPdbers113993965
MSV3drs113993965
GWAS Ctlgrs113993965
Max Magnitude0
ClinVar
Risk rs113993965(A;A)
Alt rs113993965(A;A)
Reference rs113993965(G;G)
Significance Pathogenic
Disease ADULT syndrome
Variation info
Gene TP63
CLNDBN ADULT syndrome
Reversed 0
HGVS NC_000003.11:g.189526254G>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000032229.1,