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rs121912665

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121912665(C;T)
Make rs121912665(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position7674965
GeneTP53
is asnp
is mentioned by
dbSNPrs121912665
ebirs121912665
HLIrs121912665
Exacrs121912665
Varsomers121912665
Maprs121912665
PheGenIrs121912665
hapmaprs121912665
1000 genomesrs121912665
hgdprs121912665
ensemblrs121912665
gopubmedrs121912665
geneviewrs121912665
scholarrs121912665
googlers121912665
pharmgkbrs121912665
gwascentralrs121912665
openSNPrs121912665
23andMers121912665
23andMe allrs121912665
SNP Nexus

SNPshotrs121912665
SNPdbers121912665
MSV3drs121912665
GWAS Ctlgrs121912665
Max Magnitude0
OMIM191170
Desc
Variant0038
Relatedalso
ClinVar
Risk rs121912665(T;T)
Alt rs121912665(T;T)
Reference rs121912665(C;C)
Significance Pathogenic
Disease Familial colorectal cancer Hereditary cancer-predisposing syndrome Li-Fraumeni syndrome 1
Variation info
Gene TP53
CLNDBN Familial colorectal cancer Hereditary cancer-predisposing syndrome Li-Fraumeni syndrome 1
Reversed 1
HGVS NC_000017.10:g.7578283G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000013182.22, RCV000132058.2, RCV000144671.1,