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rs397507877

From SNPedia

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


Make rs397507877(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32341043
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507877
dbSNP (classic)rs397507877
ClinGenrs397507877
ebirs397507877
HLIrs397507877
Exacrs397507877
Gnomadrs397507877
Varsomers397507877
LitVarrs397507877
Maprs397507877
PheGenIrs397507877
Biobankrs397507877
1000 genomesrs397507877
hgdprs397507877
ensemblrs397507877
geneviewrs397507877
scholarrs397507877
googlers397507877
pharmgkbrs397507877
gwascentralrs397507877
openSNPrs397507877
23andMers397507877
SNPshotrs397507877
SNPdbers397507877
MSV3drs397507877
GWAS Ctlgrs397507877
Max Magnitude6
ClinVar
Risk rs397507877(-;-)
Alt rs397507877(-;-)
Reference Rs397507877(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.32915180delA
CLNSRC ClinVar
CLNACC RCV000045019.2, RCV000240978.2,