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rs587782605

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;AA) 6 BRCA2 variant considered pathogenic for breast cancer
(AA;AA) 0 common in clinvar


Make rs587782605(-;-)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32339825
GeneBRCA2
is asnp
is mentioned by
dbSNPrs587782605
ClinGenrs587782605
ebirs587782605
HLIrs587782605
Exacrs587782605
Varsomers587782605
Maprs587782605
PheGenIrs587782605
hapmaprs587782605
1000 genomesrs587782605
hgdprs587782605
ensemblrs587782605
gopubmedrs587782605
geneviewrs587782605
scholarrs587782605
googlers587782605
pharmgkbrs587782605
gwascentralrs587782605
openSNPrs587782605
23andMers587782605
23andMe allrs587782605
SNP Nexus

SNPshotrs587782605
SNPdbers587782605
MSV3drs587782605
GWAS Ctlgrs587782605
Max Magnitude6
ClinVar
Risk rs587782605(-;-)
Alt rs587782605(-;-)
Reference Rs587782605(AA;AA)
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.32913962_32913963delAA
CLNSRC
CLNACC RCV000131974.2, RCV000241399.1,