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rs879255469

From SNPedia

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


Make rs879255469(-;-)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32363514
GeneBRCA2
is asnp
is mentioned by
dbSNPrs879255469
dbSNP (old)rs879255469
ClinGenrs879255469
ebirs879255469
HLIrs879255469
Exacrs879255469
Gnomadrs879255469
Varsomers879255469
Maprs879255469
PheGenIrs879255469
Biobankrs879255469
1000 genomesrs879255469
hgdprs879255469
ensemblrs879255469
gopubmedrs879255469
geneviewrs879255469
scholarrs879255469
googlers879255469
pharmgkbrs879255469
gwascentralrs879255469
openSNPrs879255469
23andMers879255469
23andMe allrs879255469
SNP Nexus

SNPshotrs879255469
SNPdbers879255469
MSV3drs879255469
GWAS Ctlgrs879255469
Max Magnitude6
ClinVar
Risk rs879255469(-;-)
Alt rs879255469(-;-)
Reference Rs879255469(C;C)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32937651delC
CLNSRC
CLNACC RCV000239308.2,