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rs397507586

From SNPedia

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


Make rs397507586(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32332883
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507586
dbSNP (old)rs397507586
ClinGenrs397507586
ebirs397507586
HLIrs397507586
Exacrs397507586
Gnomadrs397507586
Varsomers397507586
Maprs397507586
PheGenIrs397507586
Biobankrs397507586
1000 genomesrs397507586
hgdprs397507586
ensemblrs397507586
gopubmedrs397507586
geneviewrs397507586
scholarrs397507586
googlers397507586
pharmgkbrs397507586
gwascentralrs397507586
openSNPrs397507586
23andMers397507586
23andMe allrs397507586
SNP Nexus

SNPshotrs397507586
SNPdbers397507586
MSV3drs397507586
GWAS Ctlgrs397507586
Max Magnitude6
ClinVar
Risk rs397507586(-;-)
Alt rs397507586(-;-)
Reference Rs397507586(AG;AG)
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.32907020_32907021delGA
CLNSRC ClinVar
CLNACC RCV000043800.2, RCV000257191.2,