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rs397507896

From SNPedia

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


Make rs397507896(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32354945
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507896
dbSNP (old)rs397507896
ClinGenrs397507896
ebirs397507896
HLIrs397507896
Exacrs397507896
Gnomadrs397507896
Varsomers397507896
Maprs397507896
PheGenIrs397507896
Biobankrs397507896
1000 genomesrs397507896
hgdprs397507896
ensemblrs397507896
gopubmedrs397507896
geneviewrs397507896
scholarrs397507896
googlers397507896
pharmgkbrs397507896
gwascentralrs397507896
openSNPrs397507896
23andMers397507896
23andMe allrs397507896
SNP Nexus

SNPshotrs397507896
SNPdbers397507896
MSV3drs397507896
GWAS Ctlgrs397507896
Max Magnitude6
ClinVar
Risk rs397507896(-;-)
Alt rs397507896(-;-)
Reference Rs397507896(A;A)
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.32929082delA
CLNSRC ClinVar
CLNACC RCV000045141.2, RCV000241029.2,