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rs587782590

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587782590(A;A)
Make rs587782590(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32325185
GeneBRCA2
is asnp
is mentioned by
dbSNPrs587782590
ebirs587782590
HLIrs587782590
Exacrs587782590
Varsomers587782590
Maprs587782590
PheGenIrs587782590
hapmaprs587782590
1000 genomesrs587782590
hgdprs587782590
ensemblrs587782590
gopubmedrs587782590
geneviewrs587782590
scholarrs587782590
googlers587782590
pharmgkbrs587782590
gwascentralrs587782590
openSNPrs587782590
23andMers587782590
23andMe allrs587782590
SNP Nexus

SNPshotrs587782590
SNPdbers587782590
MSV3drs587782590
GWAS Ctlgrs587782590
Max Magnitude0
ClinVar
Risk rs587782590(A;A)
Alt rs587782590(A;A)
Reference rs587782590(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32899322G>A
CLNSRC
CLNACC RCV000131929.2,