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

rs876659482

From SNPedia

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


Make rs876659482(-;-)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32339712
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876659482
ClinGenrs876659482
ebirs876659482
HLIrs876659482
Exacrs876659482
Varsomers876659482
Maprs876659482
PheGenIrs876659482
hapmaprs876659482
1000 genomesrs876659482
hgdprs876659482
ensemblrs876659482
gopubmedrs876659482
geneviewrs876659482
scholarrs876659482
googlers876659482
pharmgkbrs876659482
gwascentralrs876659482
openSNPrs876659482
23andMers876659482
23andMe allrs876659482
SNP Nexus

SNPshotrs876659482
SNPdbers876659482
MSV3drs876659482
GWAS Ctlgrs876659482
Max Magnitude6
ClinVar
Risk rs876659482(-;-)
Alt rs876659482(-;-)
Reference Rs876659482(G;G)
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.32913849delG
CLNSRC
CLNACC RCV000213290.1, RCV000257609.2,