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rs587780659

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587780659(-;-)
Make rs587780659(-;A)
Make rs587780659(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32340917
GeneBRCA2
is asnp
is mentioned by
dbSNPrs587780659
ebirs587780659
HLIrs587780659
Exacrs587780659
Varsomers587780659
Maprs587780659
PheGenIrs587780659
hapmaprs587780659
1000 genomesrs587780659
hgdprs587780659
ensemblrs587780659
gopubmedrs587780659
geneviewrs587780659
scholarrs587780659
googlers587780659
pharmgkbrs587780659
gwascentralrs587780659
openSNPrs587780659
23andMers587780659
23andMe allrs587780659
SNP Nexus

SNPshotrs587780659
SNPdbers587780659
MSV3drs587780659
GWAS Ctlgrs587780659
Max Magnitude0
ClinVar
Risk rs587780659(A;A)
Alt rs587780659(A;A)
Reference rs587780659(;)
Significance Pathogenic
Disease Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome Familial cancer of breast Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome Familial cancer of breast Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000013.10:g.32915058dupA
CLNSRC
CLNACC RCV000031635.3, RCV000122925.1, RCV000160303.1, RCV000214634.1,