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rs397507734

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


Make rs397507734(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339002
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507734
dbSNP (old)rs397507734
ClinGenrs397507734
ebirs397507734
HLIrs397507734
Exacrs397507734
Gnomadrs397507734
Varsomers397507734
Maprs397507734
PheGenIrs397507734
Biobankrs397507734
1000 genomesrs397507734
hgdprs397507734
ensemblrs397507734
gopubmedrs397507734
geneviewrs397507734
scholarrs397507734
googlers397507734
pharmgkbrs397507734
gwascentralrs397507734
openSNPrs397507734
23andMers397507734
23andMe allrs397507734
SNP Nexus

SNPshotrs397507734
SNPdbers397507734
MSV3drs397507734
GWAS Ctlgrs397507734
Max Magnitude6
ClinVar
Risk rs397507734(-;-)
Alt rs397507734(-;-)
Reference Rs397507734(AGAG;AGAG)
Significance Pathogenic
Disease Familial cancer of breast Hereditary cancer-predisposing syndrome Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32913139_32913142delAGAG
CLNSRC ClinVar
CLNACC RCV000044459.2, RCV000165672.2, RCV000238961.3,