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rs397507935

From SNPedia

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


Make rs397507935(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32357831
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507935
dbSNP (old)rs397507935
ClinGenrs397507935
ebirs397507935
HLIrs397507935
Exacrs397507935
Gnomadrs397507935
Varsomers397507935
Maprs397507935
PheGenIrs397507935
Biobankrs397507935
1000 genomesrs397507935
hgdprs397507935
ensemblrs397507935
gopubmedrs397507935
geneviewrs397507935
scholarrs397507935
googlers397507935
pharmgkbrs397507935
gwascentralrs397507935
openSNPrs397507935
23andMers397507935
23andMe allrs397507935
SNP Nexus

SNPshotrs397507935
SNPdbers397507935
MSV3drs397507935
GWAS Ctlgrs397507935
Max Magnitude6
ClinVar
Risk rs397507935(-;-)
Alt rs397507935(-;-)
Reference Rs397507935(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.32931968delT
CLNSRC ClinVar
CLNACC RCV000045292.2, RCV000256641.2,