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rs121912658

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121912658(A;T)
Make rs121912658(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position7676011
GeneTP53
is asnp
is mentioned by
dbSNPrs121912658
ebirs121912658
HLIrs121912658
Exacrs121912658
Varsomers121912658
Maprs121912658
PheGenIrs121912658
hapmaprs121912658
1000 genomesrs121912658
hgdprs121912658
ensemblrs121912658
gopubmedrs121912658
geneviewrs121912658
scholarrs121912658
googlers121912658
pharmgkbrs121912658
gwascentralrs121912658
openSNPrs121912658
23andMers121912658
23andMe allrs121912658
SNP Nexus

SNPshotrs121912658
SNPdbers121912658
MSV3drs121912658
GWAS Ctlgrs121912658
Max Magnitude0
OMIM191170
Desc
Variant0017
Relatedalso
ClinVar
Risk rs121912658(G,T;G,T)
Alt rs121912658(G,T;G,T)
Reference rs121912658(A;A)
Significance Pathogenic
Disease Li-Fraumeni-like syndrome Hereditary cancer-predisposing syndrome not provided
Variation info
Gene TP53
CLNDBN Li-Fraumeni-like syndrome Hereditary cancer-predisposing syndrome not provided
Reversed 1
HGVS NC_000017.10:g.7579329T>A; NC_000017.10:g.7579329T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000013158.22, RCV000129457.5, RCV000213049.1,