Have questions? Visit https://www.reddit.com/r/SNPedia

rs397507694

From SNPedia

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


Make rs397507694(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32338221
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507694
dbSNP (old)rs397507694
ClinGenrs397507694
ebirs397507694
HLIrs397507694
Exacrs397507694
Gnomadrs397507694
Varsomers397507694
Maprs397507694
PheGenIrs397507694
Biobankrs397507694
1000 genomesrs397507694
hgdprs397507694
ensemblrs397507694
gopubmedrs397507694
geneviewrs397507694
scholarrs397507694
googlers397507694
pharmgkbrs397507694
gwascentralrs397507694
openSNPrs397507694
23andMers397507694
23andMe allrs397507694
SNP Nexus

SNPshotrs397507694
SNPdbers397507694
MSV3drs397507694
GWAS Ctlgrs397507694
Max Magnitude6
ClinVar
Risk rs397507694(-;-)
Alt rs397507694(-;-)
Reference Rs397507694(AA;AA)
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.32912358_32912359delAA
CLNSRC ClinVar
CLNACC RCV000044293.2, RCV000257656.2,