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rs397508051

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508051(-;-)
Make rs397508051(-;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position32394863
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508051
ebirs397508051
HLIrs397508051
Exacrs397508051
Varsomers397508051
Maprs397508051
PheGenIrs397508051
hapmaprs397508051
1000 genomesrs397508051
hgdprs397508051
ensemblrs397508051
gopubmedrs397508051
geneviewrs397508051
scholarrs397508051
googlers397508051
pharmgkbrs397508051
gwascentralrs397508051
openSNPrs397508051
23andMers397508051
23andMe allrs397508051
SNP Nexus

SNPshotrs397508051
SNPdbers397508051
MSV3drs397508051
GWAS Ctlgrs397508051
Max Magnitude0
ClinVar
Risk rs397508051(;)
Alt rs397508051(;)
Reference rs397508051(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.32969000delC
CLNSRC ClinVar
CLNACC RCV000045819.2,