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rs397507892

From SNPedia

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


Make rs397507892(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32330939
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507892
dbSNP (old)rs397507892
ClinGenrs397507892
ebirs397507892
HLIrs397507892
Exacrs397507892
Gnomadrs397507892
Varsomers397507892
Maprs397507892
PheGenIrs397507892
Biobankrs397507892
1000 genomesrs397507892
hgdprs397507892
ensemblrs397507892
gopubmedrs397507892
geneviewrs397507892
scholarrs397507892
googlers397507892
pharmgkbrs397507892
gwascentralrs397507892
openSNPrs397507892
23andMers397507892
23andMe allrs397507892
SNP Nexus

SNPshotrs397507892
SNPdbers397507892
MSV3drs397507892
GWAS Ctlgrs397507892
Max Magnitude6
ClinVar
Risk rs397507892(-;-)
Alt rs397507892(-;-)
Reference Rs397507892(C;C)
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.32905076delC
CLNSRC ClinVar
CLNACC RCV000045124.2, RCV000257567.2,