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rs397507734

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AGAG;AGAG) 0 common in clinvar
Make rs397507734(-;-)
Make rs397507734(-;AGAG)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339002
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507734
ebirs397507734
HLIrs397507734
Exacrs397507734
Varsomers397507734
Maprs397507734
PheGenIrs397507734
hapmaprs397507734
1000 genomesrs397507734
hgdprs397507734
ensemblrs397507734
gopubmedrs397507734
geneviewrs397507734
scholarrs397507734
googlers397507734
pharmgkbrs397507734
gwascentralrs397507734
openSNPrs397507734
23andMers397507734
23andMe allrs397507734
SNP Nexus

SNPshotrs397507734
SNPdbers397507734
MSV3drs397507734
GWAS Ctlgrs397507734
Max Magnitude0
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, RCV000165672.1, RCV000238961.1,