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rs397507872

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GT;GT) 0 common in clinvar
(TG;TG) 0 common in clinvar
Make rs397507872(-;-)
Make rs397507872(-;GT)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340990
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507872
ebirs397507872
HLIrs397507872
Exacrs397507872
Varsomers397507872
Maprs397507872
PheGenIrs397507872
hapmaprs397507872
1000 genomesrs397507872
hgdprs397507872
ensemblrs397507872
gopubmedrs397507872
geneviewrs397507872
scholarrs397507872
googlers397507872
pharmgkbrs397507872
gwascentralrs397507872
openSNPrs397507872
23andMers397507872
23andMe allrs397507872
SNP Nexus

SNPshotrs397507872
SNPdbers397507872
MSV3drs397507872
GWAS Ctlgrs397507872
Max Magnitude0
ClinVar
Risk rs397507872(;)
Alt rs397507872(;)
Reference rs397507872(TG;TG)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32915127_32915128delGT
CLNSRC ClinVar
CLNACC RCV000045000.2,