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rs587782650

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587782650(C;GT)
Make rs587782650(GT;GT)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position7676232
GeneTP53
is asnp
is mentioned by
dbSNPrs587782650
ebirs587782650
HLIrs587782650
Exacrs587782650
Varsomers587782650
Maprs587782650
PheGenIrs587782650
hapmaprs587782650
1000 genomesrs587782650
hgdprs587782650
ensemblrs587782650
gopubmedrs587782650
geneviewrs587782650
scholarrs587782650
googlers587782650
pharmgkbrs587782650
gwascentralrs587782650
openSNPrs587782650
23andMers587782650
23andMe allrs587782650
SNP Nexus

SNPshotrs587782650
SNPdbers587782650
MSV3drs587782650
GWAS Ctlgrs587782650
Max Magnitude0
ClinVar
Risk rs587782650(GT;GT)
Alt rs587782650(GT;GT)
Reference rs587782650(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene TP53
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.7579550delGinsAC
CLNSRC
CLNACC RCV000132061.2,