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rs397508054

From SNPedia

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


Make rs397508054(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32394906
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508054
dbSNP (old)rs397508054
ClinGenrs397508054
ebirs397508054
HLIrs397508054
Exacrs397508054
Gnomadrs397508054
Varsomers397508054
Maprs397508054
PheGenIrs397508054
Biobankrs397508054
1000 genomesrs397508054
hgdprs397508054
ensemblrs397508054
gopubmedrs397508054
geneviewrs397508054
scholarrs397508054
googlers397508054
pharmgkbrs397508054
gwascentralrs397508054
openSNPrs397508054
23andMers397508054
23andMe allrs397508054
SNP Nexus

SNPshotrs397508054
SNPdbers397508054
MSV3drs397508054
GWAS Ctlgrs397508054
Max Magnitude6
ClinVar
Risk rs397508054(-;-)
Alt rs397508054(-;-)
Reference Rs397508054(A;A)
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.32969043delA
CLNSRC ClinVar
CLNACC RCV000045830.2, RCV000257243.2,