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rs587782272

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587782272(A;A)
Make rs587782272(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position7670716
GeneTP53
is asnp
is mentioned by
dbSNPrs587782272
ebirs587782272
HLIrs587782272
Exacrs587782272
Varsomers587782272
Maprs587782272
PheGenIrs587782272
hapmaprs587782272
1000 genomesrs587782272
hgdprs587782272
ensemblrs587782272
gopubmedrs587782272
geneviewrs587782272
scholarrs587782272
googlers587782272
pharmgkbrs587782272
gwascentralrs587782272
openSNPrs587782272
23andMers587782272
23andMe allrs587782272
SNP Nexus

SNPshotrs587782272
SNPdbers587782272
MSV3drs587782272
GWAS Ctlgrs587782272
Max Magnitude0
ClinVar
Risk rs587782272(A,C;A,C)
Alt rs587782272(A,C;A,C)
Reference rs587782272(G;G)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations Hereditary cancer-predisposing syndrome
Variation info
Gene TP53
CLNDBN Tumor susceptibility linked to germline BAP1 mutations Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.7574034C>G; NC_000017.10:g.7574034C>T
CLNSRC
CLNACC RCV000221716.1, RCV000131124.2,