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rs397507596

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs397507596(-;-)
Make rs397507596(-;AA)
ReferenceGRCh38 38.1/141
Chromosome13
Position32333074
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507596
ebirs397507596
HLIrs397507596
Exacrs397507596
Varsomers397507596
Maprs397507596
PheGenIrs397507596
hapmaprs397507596
1000 genomesrs397507596
hgdprs397507596
ensemblrs397507596
gopubmedrs397507596
geneviewrs397507596
scholarrs397507596
googlers397507596
pharmgkbrs397507596
gwascentralrs397507596
openSNPrs397507596
23andMers397507596
23andMe allrs397507596
SNP Nexus

SNPshotrs397507596
SNPdbers397507596
MSV3drs397507596
GWAS Ctlgrs397507596
Max Magnitude0
ClinVar
Risk rs397507596(;)
Alt rs397507596(;)
Reference rs397507596(AA;AA)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32907211_32907212delAA
CLNSRC ClinVar
CLNACC RCV000043837.2,