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rs397507945

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397507945(-;-)
Make rs397507945(-;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position32362680
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507945
ebirs397507945
HLIrs397507945
Exacrs397507945
Varsomers397507945
Maprs397507945
PheGenIrs397507945
hapmaprs397507945
1000 genomesrs397507945
hgdprs397507945
ensemblrs397507945
gopubmedrs397507945
geneviewrs397507945
scholarrs397507945
googlers397507945
pharmgkbrs397507945
gwascentralrs397507945
openSNPrs397507945
23andMers397507945
23andMe allrs397507945
SNP Nexus

SNPshotrs397507945
SNPdbers397507945
MSV3drs397507945
GWAS Ctlgrs397507945
Max Magnitude0
ClinVar
Risk rs397507945(;)
Alt rs397507945(;)
Reference rs397507945(C;C)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32936817delC
CLNSRC ClinVar
CLNACC RCV000045358.2,