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rs587782705

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587782705(C;T)
Make rs587782705(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position7675157
GeneTP53
is asnp
is mentioned by
dbSNPrs587782705
ebirs587782705
HLIrs587782705
Exacrs587782705
Varsomers587782705
Maprs587782705
PheGenIrs587782705
hapmaprs587782705
1000 genomesrs587782705
hgdprs587782705
ensemblrs587782705
gopubmedrs587782705
geneviewrs587782705
scholarrs587782705
googlers587782705
pharmgkbrs587782705
gwascentralrs587782705
openSNPrs587782705
23andMers587782705
23andMe allrs587782705
SNP Nexus

SNPshotrs587782705
SNPdbers587782705
MSV3drs587782705
GWAS Ctlgrs587782705
Max Magnitude0
ClinVar
Risk rs587782705(T;T)
Alt rs587782705(T;T)
Reference rs587782705(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Li-Fraumeni syndrome
Variation info
Gene TP53
CLNDBN Hereditary cancer-predisposing syndrome Li-Fraumeni syndrome
Reversed 1
HGVS NC_000017.10:g.7578475G>A
CLNSRC
CLNACC RCV000132156.4, RCV000168122.2,