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rs397507782

From SNPedia

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


Make rs397507782(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339735
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507782
dbSNP (old)rs397507782
ClinGenrs397507782
ebirs397507782
HLIrs397507782
Exacrs397507782
Varsomers397507782
Maprs397507782
PheGenIrs397507782
Biobankrs397507782
1000 genomesrs397507782
hgdprs397507782
ensemblrs397507782
gopubmedrs397507782
geneviewrs397507782
scholarrs397507782
googlers397507782
pharmgkbrs397507782
gwascentralrs397507782
openSNPrs397507782
23andMers397507782
23andMe allrs397507782
SNP Nexus

SNPshotrs397507782
SNPdbers397507782
MSV3drs397507782
GWAS Ctlgrs397507782
Max Magnitude6
ClinVar
Risk rs397507782(-;-)
Alt rs397507782(-;-)
Reference Rs397507782(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.32913872delG
CLNSRC ClinVar
CLNACC RCV000044645.2, RCV000257237.1,