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rs397507936

From SNPedia

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


Make rs397507936(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32357875
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507936
dbSNP (old)rs397507936
ClinGenrs397507936
ebirs397507936
HLIrs397507936
Exacrs397507936
Gnomadrs397507936
Varsomers397507936
Maprs397507936
PheGenIrs397507936
Biobankrs397507936
1000 genomesrs397507936
hgdprs397507936
ensemblrs397507936
gopubmedrs397507936
geneviewrs397507936
scholarrs397507936
googlers397507936
pharmgkbrs397507936
gwascentralrs397507936
openSNPrs397507936
23andMers397507936
23andMe allrs397507936
SNP Nexus

SNPshotrs397507936
SNPdbers397507936
MSV3drs397507936
GWAS Ctlgrs397507936
Max Magnitude6
ClinVar
Risk rs397507936(-;-)
Alt rs397507936(-;-)
Reference Rs397507936(G;G)
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.32932012delG
CLNSRC ClinVar
CLNACC RCV000045300.2, RCV000257037.1,