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rs587781525

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587781525(A;G)
Make rs587781525(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position7673778
GeneTP53
is asnp
is mentioned by
dbSNPrs587781525
ebirs587781525
HLIrs587781525
Exacrs587781525
Varsomers587781525
Maprs587781525
PheGenIrs587781525
hapmaprs587781525
1000 genomesrs587781525
hgdprs587781525
ensemblrs587781525
gopubmedrs587781525
geneviewrs587781525
scholarrs587781525
googlers587781525
pharmgkbrs587781525
gwascentralrs587781525
openSNPrs587781525
23andMers587781525
23andMe allrs587781525
SNP Nexus

SNPshotrs587781525
SNPdbers587781525
MSV3drs587781525
GWAS Ctlgrs587781525
Max Magnitude0
ClinVar
Risk rs587781525(G,T;G,T)
Alt rs587781525(G,T;G,T)
Reference rs587781525(A;A)
Significance Pathogenic
Disease not provided Tumor susceptibility linked to germline BAP1 mutations Hereditary cancer-predisposing syndrome
Variation info
Gene TP53
CLNDBN not provided Tumor susceptibility linked to germline BAP1 mutations Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.7577096T>A; NC_000017.10:g.7577096T>C
CLNSRC
CLNACC RCV000161072.1, RCV000215048.1, RCV000129516.2,