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rs397507593

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
(-;G) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs397507593(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32333018
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507593
dbSNP (old)rs397507593
ClinGenrs397507593
ebirs397507593
HLIrs397507593
Exacrs397507593
Gnomadrs397507593
Varsomers397507593
Maprs397507593
PheGenIrs397507593
Biobankrs397507593
1000 genomesrs397507593
hgdprs397507593
ensemblrs397507593
gopubmedrs397507593
geneviewrs397507593
scholarrs397507593
googlers397507593
pharmgkbrs397507593
gwascentralrs397507593
openSNPrs397507593
23andMers397507593
23andMe allrs397507593
SNP Nexus

SNPshotrs397507593
SNPdbers397507593
MSV3drs397507593
GWAS Ctlgrs397507593
Max Magnitude6
ClinVar
Risk rs397507593(G;G)
Alt rs397507593(G;G)
Reference Rs397507593(-;-)
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.32907155dupG
CLNSRC ClinVar
CLNACC RCV000043824.2, RCV000257403.2,