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rs397507885

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507885(-;-)
Make rs397507885(-;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32341169
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507885
ebirs397507885
HLIrs397507885
Exacrs397507885
Varsomers397507885
Maprs397507885
PheGenIrs397507885
hapmaprs397507885
1000 genomesrs397507885
hgdprs397507885
ensemblrs397507885
gopubmedrs397507885
geneviewrs397507885
scholarrs397507885
googlers397507885
pharmgkbrs397507885
gwascentralrs397507885
openSNPrs397507885
23andMers397507885
23andMe allrs397507885
SNP Nexus

SNPshotrs397507885
SNPdbers397507885
MSV3drs397507885
GWAS Ctlgrs397507885
Max Magnitude0
ClinVar
Risk rs397507885(;)
Alt rs397507885(;)
Reference rs397507885(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.32915306delA
CLNSRC ClinVar
CLNACC RCV000045060.2,