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rs879255457

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs879255457(-;-)
Make rs879255457(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32339596
GeneBRCA2
is asnp
is mentioned by
dbSNPrs879255457
dbSNP (classic)rs879255457
ClinGenrs879255457
ebirs879255457
HLIrs879255457
Exacrs879255457
Gnomadrs879255457
Varsomers879255457
LitVarrs879255457
Maprs879255457
PheGenIrs879255457
Biobankrs879255457
1000 genomesrs879255457
hgdprs879255457
ensemblrs879255457
geneviewrs879255457
scholarrs879255457
googlers879255457
pharmgkbrs879255457
gwascentralrs879255457
openSNPrs879255457
23andMers879255457
SNPshotrs879255457
SNPdbers879255457
MSV3drs879255457
GWAS Ctlgrs879255457
Max Magnitude0
ClinVar
Risk rs879255457(-;-)
Alt rs879255457(-;-)
Reference Rs879255457(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.32913733delC
CLNSRC
CLNACC RCV000239271.1,