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rs398122541

From SNPedia

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


Make rs398122541(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340197
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122541
dbSNP (classic)rs398122541
ClinGenrs398122541
ebirs398122541
HLIrs398122541
Exacrs398122541
Gnomadrs398122541
Varsomers398122541
LitVarrs398122541
Maprs398122541
PheGenIrs398122541
Biobankrs398122541
1000 genomesrs398122541
hgdprs398122541
ensemblrs398122541
geneviewrs398122541
scholarrs398122541
googlers398122541
pharmgkbrs398122541
gwascentralrs398122541
openSNPrs398122541
23andMers398122541
SNPshotrs398122541
SNPdbers398122541
MSV3drs398122541
GWAS Ctlgrs398122541
Max Magnitude6
ClinVar
Risk rs398122541(-;-)
Alt rs398122541(-;-)
Reference Rs398122541(T;T)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32914334delT
CLNSRC ClinVar
CLNACC RCV000076943.3,