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rs879255442

From SNPedia

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


Make rs879255442(-;-)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32336599
GeneBRCA2
is asnp
is mentioned by
dbSNPrs879255442
ClinGenrs879255442
ebirs879255442
HLIrs879255442
Exacrs879255442
Varsomers879255442
Maprs879255442
PheGenIrs879255442
Biobankrs879255442
1000 genomesrs879255442
hgdprs879255442
ensemblrs879255442
gopubmedrs879255442
geneviewrs879255442
scholarrs879255442
googlers879255442
pharmgkbrs879255442
gwascentralrs879255442
openSNPrs879255442
23andMers879255442
23andMe allrs879255442
SNP Nexus

SNPshotrs879255442
SNPdbers879255442
MSV3drs879255442
GWAS Ctlgrs879255442
Max Magnitude6
ClinVar
Risk rs879255442(-;-)
Alt rs879255442(-;-)
Reference Rs879255442(AC;AC)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32910736_32910737delCA
CLNSRC
CLNACC RCV000238671.2,