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rs397508020

From SNPedia

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


Make rs397508020(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32379486
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508020
dbSNP (old)rs397508020
ClinGenrs397508020
ebirs397508020
HLIrs397508020
Exacrs397508020
Varsomers397508020
Maprs397508020
PheGenIrs397508020
Biobankrs397508020
1000 genomesrs397508020
hgdprs397508020
ensemblrs397508020
gopubmedrs397508020
geneviewrs397508020
scholarrs397508020
googlers397508020
pharmgkbrs397508020
gwascentralrs397508020
openSNPrs397508020
23andMers397508020
23andMe allrs397508020
SNP Nexus

SNPshotrs397508020
SNPdbers397508020
MSV3drs397508020
GWAS Ctlgrs397508020
Max Magnitude6
ClinVar
Risk rs397508020(-;-)
Alt rs397508020(-;-)
Reference Rs397508020(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.32953623delT
CLNSRC ClinVar
CLNACC RCV000045659.2, RCV000257521.2,