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rs121912659

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121912659(G;T)
Make rs121912659(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position7673554
GeneTP53
is asnp
is mentioned by
dbSNPrs121912659
ebirs121912659
HLIrs121912659
Exacrs121912659
Varsomers121912659
Maprs121912659
PheGenIrs121912659
hapmaprs121912659
1000 genomesrs121912659
hgdprs121912659
ensemblrs121912659
gopubmedrs121912659
geneviewrs121912659
scholarrs121912659
googlers121912659
pharmgkbrs121912659
gwascentralrs121912659
openSNPrs121912659
23andMers121912659
23andMe allrs121912659
SNP Nexus

SNPshotrs121912659
SNPdbers121912659
MSV3drs121912659
GWAS Ctlgrs121912659
Merged fromRs28934271
Max Magnitude0
OMIM191170
Desc
Variant0021
Relatedalso
ClinVar
Risk rs121912659(T;T)
Alt rs121912659(T;T)
Reference rs121912659(G;G)
Significance Pathogenic
Disease Malignant lymphoma Familial colorectal cancer Hereditary cancer-predisposing syndrome Li-Fraumeni syndrome not specified
Variation info
Gene TP53
CLNDBN Malignant lymphoma, non-Hodgkin Familial colorectal cancer Hereditary cancer-predisposing syndrome Li-Fraumeni syndrome not specified
Reversed 1
HGVS NC_000017.10:g.7576872C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000013165.24, RCV000013166.23, RCV000131411.2, RCV000232570.1, RCV000236768.1,