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rs397507880

From SNPedia

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


Make rs397507880(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32329484
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507880
dbSNP (old)rs397507880
ClinGenrs397507880
ebirs397507880
HLIrs397507880
Exacrs397507880
Gnomadrs397507880
Varsomers397507880
Maprs397507880
PheGenIrs397507880
Biobankrs397507880
1000 genomesrs397507880
hgdprs397507880
ensemblrs397507880
gopubmedrs397507880
geneviewrs397507880
scholarrs397507880
googlers397507880
pharmgkbrs397507880
gwascentralrs397507880
openSNPrs397507880
23andMers397507880
23andMe allrs397507880
SNP Nexus

SNPshotrs397507880
SNPdbers397507880
MSV3drs397507880
GWAS Ctlgrs397507880
Max Magnitude6
ClinVar
Risk rs397507880(-;-)
Alt rs397507880(-;-)
Reference Rs397507880(ACTA;ACTA)
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.32903621_32903624delACTA
CLNSRC ClinVar
CLNACC RCV000045036.2, RCV000257710.2,