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rs587779362

From SNPedia

Orientationplus
Geno Mag Summary
(GA;GA) 0 common in clinvar
Make rs587779362(GA;TT)
Make rs587779362(TT;TT)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32337430
GeneBRCA2
is asnp
is mentioned by
dbSNPrs587779362
ebirs587779362
HLIrs587779362
Exacrs587779362
Varsomers587779362
Maprs587779362
PheGenIrs587779362
hapmaprs587779362
1000 genomesrs587779362
hgdprs587779362
ensemblrs587779362
gopubmedrs587779362
geneviewrs587779362
scholarrs587779362
googlers587779362
pharmgkbrs587779362
gwascentralrs587779362
openSNPrs587779362
23andMers587779362
23andMe allrs587779362
SNP Nexus

SNPshotrs587779362
SNPdbers587779362
MSV3drs587779362
GWAS Ctlgrs587779362
Max Magnitude0
ClinVar
Risk rs587779362(TT;TT)
Alt rs587779362(TT;TT)
Reference rs587779362(GA;GA)
Significance Pathogenic
Disease Familial cancer of breast Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32911567_32911568delGAinsTT
CLNSRC
CLNACC RCV000074523.3, RCV000165145.1, RCV000205398.1, RCV000239127.1,