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rs397507811

From SNPedia

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


Make rs397507811(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340253
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507811
dbSNP (old)rs397507811
ClinGenrs397507811
ebirs397507811
HLIrs397507811
Exacrs397507811
Gnomadrs397507811
Varsomers397507811
Maprs397507811
PheGenIrs397507811
Biobankrs397507811
1000 genomesrs397507811
hgdprs397507811
ensemblrs397507811
gopubmedrs397507811
geneviewrs397507811
scholarrs397507811
googlers397507811
pharmgkbrs397507811
gwascentralrs397507811
openSNPrs397507811
23andMers397507811
23andMe allrs397507811
SNP Nexus

SNPshotrs397507811
SNPdbers397507811
MSV3drs397507811
GWAS Ctlgrs397507811
Max Magnitude6
ClinVar
Risk rs397507811(-;-)
Alt rs397507811(-;-)
Reference Rs397507811(T;T)
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.32914390delT
CLNSRC ClinVar
CLNACC RCV000044789.2, RCV000257211.2,