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rs397507968

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507968(-;-)
Make rs397507968(-;C)
Make rs397507968(C;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position32363408
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507968
ebirs397507968
HLIrs397507968
Exacrs397507968
Varsomers397507968
Maprs397507968
PheGenIrs397507968
hapmaprs397507968
1000 genomesrs397507968
hgdprs397507968
ensemblrs397507968
gopubmedrs397507968
geneviewrs397507968
scholarrs397507968
googlers397507968
pharmgkbrs397507968
gwascentralrs397507968
openSNPrs397507968
23andMers397507968
23andMe allrs397507968
SNP Nexus

SNPshotrs397507968
SNPdbers397507968
MSV3drs397507968
GWAS Ctlgrs397507968
Max Magnitude0
ClinVar
Risk rs397507968(C;C)
Alt rs397507968(C;C)
Reference rs397507968(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32937545dupC
CLNSRC ClinVar
CLNACC RCV000045451.2,