Have questions? Visit https://www.reddit.com/r/SNPedia

rs876659606

From SNPedia

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


Make rs876659606(-;-)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32363211
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876659606
ClinGenrs876659606
ebirs876659606
HLIrs876659606
Exacrs876659606
Varsomers876659606
Maprs876659606
PheGenIrs876659606
hapmaprs876659606
1000 genomesrs876659606
hgdprs876659606
ensemblrs876659606
gopubmedrs876659606
geneviewrs876659606
scholarrs876659606
googlers876659606
pharmgkbrs876659606
gwascentralrs876659606
openSNPrs876659606
23andMers876659606
23andMe allrs876659606
SNP Nexus

SNPshotrs876659606
SNPdbers876659606
MSV3drs876659606
GWAS Ctlgrs876659606
Max Magnitude6
ClinVar
Risk rs876659606(-;-)
Alt rs876659606(-;-)
Reference Rs876659606(C;C)
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.32937348delC
CLNSRC
CLNACC RCV000215208.1, RCV000256797.2,