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rs869312782

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312782(G;T)
Make rs869312782(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position7676167
GeneTP53
is asnp
is mentioned by
dbSNPrs869312782
ebirs869312782
HLIrs869312782
Exacrs869312782
Varsomers869312782
Maprs869312782
PheGenIrs869312782
hapmaprs869312782
1000 genomesrs869312782
hgdprs869312782
ensemblrs869312782
gopubmedrs869312782
geneviewrs869312782
scholarrs869312782
googlers869312782
pharmgkbrs869312782
gwascentralrs869312782
openSNPrs869312782
23andMers869312782
23andMe allrs869312782
SNP Nexus

SNPshotrs869312782
SNPdbers869312782
MSV3drs869312782
GWAS Ctlgrs869312782
Max Magnitude0
ClinVar
Risk rs869312782(T;T)
Alt rs869312782(T;T)
Reference rs869312782(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene TP53
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.7579485C>A
CLNSRC
CLNACC RCV000210192.1,