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rs879255463

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
(-;A) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs879255463(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32357778
GeneBRCA2
is asnp
is mentioned by
dbSNPrs879255463
dbSNP (classic)rs879255463
ClinGenrs879255463
ebirs879255463
HLIrs879255463
Exacrs879255463
Gnomadrs879255463
Varsomers879255463
LitVarrs879255463
Maprs879255463
PheGenIrs879255463
Biobankrs879255463
1000 genomesrs879255463
hgdprs879255463
ensemblrs879255463
geneviewrs879255463
scholarrs879255463
googlers879255463
pharmgkbrs879255463
gwascentralrs879255463
openSNPrs879255463
23andMers879255463
SNPshotrs879255463
SNPdbers879255463
MSV3drs879255463
GWAS Ctlgrs879255463
Max Magnitude6
ClinVar
Risk rs879255463(A;A)
Alt rs879255463(A;A)
Reference Rs879255463(-;-)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32931915dupA
CLNSRC
CLNACC RCV000238767.2,