Have questions? Visit https://www.reddit.com/r/SNPedia

rs121912654

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121912654(G;T)
Make rs121912654(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position7675143
GeneTP53
is asnp
is mentioned by
dbSNPrs121912654
ebirs121912654
HLIrs121912654
Exacrs121912654
Varsomers121912654
Maprs121912654
PheGenIrs121912654
hapmaprs121912654
1000 genomesrs121912654
hgdprs121912654
ensemblrs121912654
gopubmedrs121912654
geneviewrs121912654
scholarrs121912654
googlers121912654
pharmgkbrs121912654
gwascentralrs121912654
openSNPrs121912654
23andMers121912654
23andMe allrs121912654
SNP Nexus

SNPshotrs121912654
SNPdbers121912654
MSV3drs121912654
GWAS Ctlgrs121912654
Max Magnitude0
OMIM191170
Desc
Variant0007
Relatedalso
ClinVar
Risk rs121912654(A,T;A,T)
Alt rs121912654(A,T;A,T)
Reference rs121912654(G;G)
Significance Pathogenic
Disease Hepatocellular carcinoma Hereditary cancer-predisposing syndrome not specified
Variation info
Gene TP53
CLNDBN Hepatocellular carcinoma Hereditary cancer-predisposing syndrome not specified
Reversed 1
HGVS NC_000017.10:g.7578461C>A; NC_000017.10:g.7578461C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013147.4, RCV000164816.1, RCV000235399.1,