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rs113993966

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs113993966(C;G)
Make rs113993966(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position189868596
GeneTP63
is asnp
is mentioned by
dbSNPrs113993966
ebirs113993966
HLIrs113993966
Exacrs113993966
Varsomers113993966
Maprs113993966
PheGenIrs113993966
hapmaprs113993966
1000 genomesrs113993966
hgdprs113993966
ensemblrs113993966
gopubmedrs113993966
geneviewrs113993966
scholarrs113993966
googlers113993966
pharmgkbrs113993966
gwascentralrs113993966
openSNPrs113993966
23andMers113993966
23andMe allrs113993966
SNP Nexus

SNPshotrs113993966
SNPdbers113993966
MSV3drs113993966
GWAS Ctlgrs113993966
Max Magnitude0
OMIM603273
Desc
Variant0022
Relatedalso
ClinVar
Risk rs113993966(G;G)
Alt rs113993966(G;G)
Reference rs113993966(C;C)
Significance Pathogenic
Disease ADULT syndrome
Variation info
Gene TP63
CLNDBN ADULT syndrome
Reversed 0
HGVS NC_000003.11:g.189586385C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000006923.2,