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rs121912655

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121912655(A;A)
Make rs121912655(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position7674238
GeneTP53
is asnp
is mentioned by
dbSNPrs121912655
ebirs121912655
HLIrs121912655
Exacrs121912655
Varsomers121912655
Maprs121912655
PheGenIrs121912655
hapmaprs121912655
1000 genomesrs121912655
hgdprs121912655
ensemblrs121912655
gopubmedrs121912655
geneviewrs121912655
scholarrs121912655
googlers121912655
pharmgkbrs121912655
gwascentralrs121912655
openSNPrs121912655
23andMers121912655
23andMe allrs121912655
SNP Nexus

SNPshotrs121912655
SNPdbers121912655
MSV3drs121912655
GWAS Ctlgrs121912655
Max Magnitude0
OMIM191170
Desc
Variant0008
Relatedalso
ClinVar
Risk rs121912655(A,C;A,C)
Alt rs121912655(A,C;A,C)
Reference rs121912655(G;G)
Significance Pathogenic
Disease Li-Fraumeni-like syndrome Hereditary cancer-predisposing syndrome Li-Fraumeni syndrome
Variation info
Gene TP53
CLNDBN Li-Fraumeni-like syndrome Hereditary cancer-predisposing syndrome Li-Fraumeni syndrome
Reversed 1
HGVS NC_000017.10:g.7577556C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013148.23, RCV000129809.2, RCV000231770.1,