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rs397508036

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508036(-;-)
Make rs397508036(-;C)
Make rs397508036(C;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position32379896
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508036
ebirs397508036
HLIrs397508036
Exacrs397508036
Varsomers397508036
Maprs397508036
PheGenIrs397508036
hapmaprs397508036
1000 genomesrs397508036
hgdprs397508036
ensemblrs397508036
gopubmedrs397508036
geneviewrs397508036
scholarrs397508036
googlers397508036
pharmgkbrs397508036
gwascentralrs397508036
openSNPrs397508036
23andMers397508036
23andMe allrs397508036
SNP Nexus

SNPshotrs397508036
SNPdbers397508036
MSV3drs397508036
GWAS Ctlgrs397508036
Max Magnitude0
ClinVar
Risk rs397508036(C;C)
Alt rs397508036(C;C)
Reference rs397508036(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32954033dupC
CLNSRC ClinVar
CLNACC RCV000045715.2,