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rs587780659

From SNPedia

Merged intors397507373
Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs587780659(-;A)
Make rs587780659(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32340917
GeneBRCA2
is asnp
is mentioned by
dbSNPrs587780659
dbSNP (classic)rs587780659
ClinGenrs587780659
ebirs587780659
HLIrs587780659
Exacrs587780659
Gnomadrs587780659
Varsomers587780659
LitVarrs587780659
Maprs587780659
PheGenIrs587780659
Biobankrs587780659
1000 genomesrs587780659
hgdprs587780659
ensemblrs587780659
geneviewrs587780659
scholarrs587780659
googlers587780659
pharmgkbrs587780659
gwascentralrs587780659
openSNPrs587780659
23andMers587780659
SNPshotrs587780659
SNPdbers587780659
MSV3drs587780659
GWAS Ctlgrs587780659
StatusMerged into rs397507373
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 Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome Familial cancer of breast Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32915058dupA
CLNSRC
CLNACC RCV000031635.5, RCV000122925.1, RCV000160303.1, RCV000214634.1,