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rs397507661

From SNPedia

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


Make rs397507661(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32337622
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507661
dbSNP (old)rs397507661
ClinGenrs397507661
ebirs397507661
HLIrs397507661
Exacrs397507661
Gnomadrs397507661
Varsomers397507661
Maprs397507661
PheGenIrs397507661
Biobankrs397507661
1000 genomesrs397507661
hgdprs397507661
ensemblrs397507661
gopubmedrs397507661
geneviewrs397507661
scholarrs397507661
googlers397507661
pharmgkbrs397507661
gwascentralrs397507661
openSNPrs397507661
23andMers397507661
23andMe allrs397507661
SNP Nexus

SNPshotrs397507661
SNPdbers397507661
MSV3drs397507661
GWAS Ctlgrs397507661
Max Magnitude6
ClinVar
Risk rs397507661(-;-)
Alt rs397507661(-;-)
Reference Rs397507661(AG;AG)
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.32911759_32911760delGA
CLNSRC ClinVar
CLNACC RCV000044165.2, RCV000257018.2,