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rs397508050

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508050(-;-)
Make rs397508050(-;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32394862
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508050
ebirs397508050
HLIrs397508050
Exacrs397508050
Varsomers397508050
Maprs397508050
PheGenIrs397508050
hapmaprs397508050
1000 genomesrs397508050
hgdprs397508050
ensemblrs397508050
gopubmedrs397508050
geneviewrs397508050
scholarrs397508050
googlers397508050
pharmgkbrs397508050
gwascentralrs397508050
openSNPrs397508050
23andMers397508050
23andMe allrs397508050
SNP Nexus

SNPshotrs397508050
SNPdbers397508050
MSV3drs397508050
GWAS Ctlgrs397508050
Max Magnitude0
ClinVar
Risk rs397508050(;)
Alt rs397508050(;)
Reference rs397508050(T;T)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32968999delT
CLNSRC ClinVar
CLNACC RCV000045818.2,