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rs397507582

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507582(-;-)
Make rs397507582(-;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32332840
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507582
ebirs397507582
HLIrs397507582
Exacrs397507582
Varsomers397507582
Maprs397507582
PheGenIrs397507582
hapmaprs397507582
1000 genomesrs397507582
hgdprs397507582
ensemblrs397507582
gopubmedrs397507582
geneviewrs397507582
scholarrs397507582
googlers397507582
pharmgkbrs397507582
gwascentralrs397507582
openSNPrs397507582
23andMers397507582
23andMe allrs397507582
SNP Nexus

SNPshotrs397507582
SNPdbers397507582
MSV3drs397507582
GWAS Ctlgrs397507582
Max Magnitude0
ClinVar
Risk rs397507582(;)
Alt rs397507582(;)
Reference rs397507582(A;A)
Significance Pathogenic
Disease Familial cancer of breast not provided Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast not provided Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32906977delA
CLNSRC ClinVar
CLNACC RCV000043789.2, RCV000236143.1, RCV000238971.1,