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rs587782613

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs587782613(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32337767
GeneBRCA2
is asnp
is mentioned by
dbSNPrs587782613
dbSNP (old)rs587782613
ClinGenrs587782613
ebirs587782613
HLIrs587782613
Exacrs587782613
Gnomadrs587782613
Varsomers587782613
Maprs587782613
PheGenIrs587782613
Biobankrs587782613
1000 genomesrs587782613
hgdprs587782613
ensemblrs587782613
gopubmedrs587782613
geneviewrs587782613
scholarrs587782613
googlers587782613
pharmgkbrs587782613
gwascentralrs587782613
openSNPrs587782613
23andMers587782613
23andMe allrs587782613
SNP Nexus

SNPshotrs587782613
SNPdbers587782613
MSV3drs587782613
GWAS Ctlgrs587782613
Max Magnitude6
ClinVar
Risk rs587782613(T;T)
Alt rs587782613(T;T)
Reference Rs587782613(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32911904C>T
CLNSRC
CLNACC RCV000131988.3, RCV000241121.2,