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rs397507799

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507799(A;CT)
Make rs397507799(CT;CT)
ReferenceGRCh38 38.1/141
Chromosome13
Position32326554
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507799
ebirs397507799
HLIrs397507799
Exacrs397507799
Varsomers397507799
Maprs397507799
PheGenIrs397507799
hapmaprs397507799
1000 genomesrs397507799
hgdprs397507799
ensemblrs397507799
gopubmedrs397507799
geneviewrs397507799
scholarrs397507799
googlers397507799
pharmgkbrs397507799
gwascentralrs397507799
openSNPrs397507799
23andMers397507799
23andMe allrs397507799
SNP Nexus

SNPshotrs397507799
SNPdbers397507799
MSV3drs397507799
GWAS Ctlgrs397507799
Max Magnitude0
ClinVar
Risk rs397507799(CT;CT)
Alt rs397507799(CT;CT)
Reference rs397507799(A;A)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32900691delAinsCT
CLNSRC ClinVar
CLNACC RCV000044736.2,