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rs587782596

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587782596(C;T)
Make rs587782596(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position7675071
GeneTP53
is asnp
is mentioned by
dbSNPrs587782596
ebirs587782596
HLIrs587782596
Exacrs587782596
Varsomers587782596
Maprs587782596
PheGenIrs587782596
hapmaprs587782596
1000 genomesrs587782596
hgdprs587782596
ensemblrs587782596
gopubmedrs587782596
geneviewrs587782596
scholarrs587782596
googlers587782596
pharmgkbrs587782596
gwascentralrs587782596
openSNPrs587782596
23andMers587782596
23andMe allrs587782596
SNP Nexus

SNPshotrs587782596
SNPdbers587782596
MSV3drs587782596
GWAS Ctlgrs587782596
Max Magnitude0
ClinVar
Risk rs587782596(A,T;A,T)
Alt rs587782596(A,T;A,T)
Reference rs587782596(C;C)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome Li-Fraumeni syndrome not specified Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene TP53
CLNDBN Hereditary cancer-predisposing syndrome Li-Fraumeni syndrome not specified Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000017.10:g.7578389G>A; NC_000017.10:g.7578389G>T
CLNSRC
CLNACC RCV000131943.2, RCV000168292.1, RCV000236276.1, RCV000222957.1,