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rs397507993

From SNPedia

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


Make rs397507993(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32371047
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507993
dbSNP (old)rs397507993
ClinGenrs397507993
ebirs397507993
HLIrs397507993
Exacrs397507993
Gnomadrs397507993
Varsomers397507993
Maprs397507993
PheGenIrs397507993
Biobankrs397507993
1000 genomesrs397507993
hgdprs397507993
ensemblrs397507993
gopubmedrs397507993
geneviewrs397507993
scholarrs397507993
googlers397507993
pharmgkbrs397507993
gwascentralrs397507993
openSNPrs397507993
23andMers397507993
23andMe allrs397507993
SNP Nexus

SNPshotrs397507993
SNPdbers397507993
MSV3drs397507993
GWAS Ctlgrs397507993
Max Magnitude6
ClinVar
Risk rs397507993(-;-)
Alt rs397507993(-;-)
Reference Rs397507993(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.32945184delA
CLNSRC ClinVar
CLNACC RCV000045565.2, RCV000256962.1,