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rs397507691

From SNPedia

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


Make rs397507691(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32338202
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507691
dbSNP (old)rs397507691
ClinGenrs397507691
ebirs397507691
HLIrs397507691
Exacrs397507691
Gnomadrs397507691
Varsomers397507691
Maprs397507691
PheGenIrs397507691
Biobankrs397507691
1000 genomesrs397507691
hgdprs397507691
ensemblrs397507691
gopubmedrs397507691
geneviewrs397507691
scholarrs397507691
googlers397507691
pharmgkbrs397507691
gwascentralrs397507691
openSNPrs397507691
23andMers397507691
23andMe allrs397507691
SNP Nexus

SNPshotrs397507691
SNPdbers397507691
MSV3drs397507691
GWAS Ctlgrs397507691
Max Magnitude6
ClinVar
Risk rs397507691(-;-)
Alt rs397507691(-;-)
Reference Rs397507691(G;G)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32912339delG
CLNSRC ClinVar
CLNACC RCV000044281.2, RCV000257712.2,