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rs397507886

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs397507886(-;-)
Make rs397507886(-;AA)
ReferenceGRCh38 38.1/141
Chromosome13
Position32341171
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507886
ebirs397507886
HLIrs397507886
Exacrs397507886
Varsomers397507886
Maprs397507886
PheGenIrs397507886
hapmaprs397507886
1000 genomesrs397507886
hgdprs397507886
ensemblrs397507886
gopubmedrs397507886
geneviewrs397507886
scholarrs397507886
googlers397507886
pharmgkbrs397507886
gwascentralrs397507886
openSNPrs397507886
23andMers397507886
23andMe allrs397507886
SNP Nexus

SNPshotrs397507886
SNPdbers397507886
MSV3drs397507886
GWAS Ctlgrs397507886
Max Magnitude0
ClinVar
Risk rs397507886(;)
Alt rs397507886(;)
Reference rs397507886(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.32915308_32915309delAA
CLNSRC ClinVar
CLNACC RCV000045061.2,