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rs397508058

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508058(A;A)
Make rs397508058(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32394934
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508058
ebirs397508058
HLIrs397508058
Exacrs397508058
Varsomers397508058
Maprs397508058
PheGenIrs397508058
hapmaprs397508058
1000 genomesrs397508058
hgdprs397508058
ensemblrs397508058
gopubmedrs397508058
geneviewrs397508058
scholarrs397508058
googlers397508058
pharmgkbrs397508058
gwascentralrs397508058
openSNPrs397508058
23andMers397508058
23andMe allrs397508058
SNP Nexus

SNPshotrs397508058
SNPdbers397508058
MSV3drs397508058
GWAS Ctlgrs397508058
Max Magnitude0
ClinVar
Risk rs397508058(A;A)
Alt rs397508058(A;A)
Reference rs397508058(G;G)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32969071G>A
CLNSRC ClinVar
CLNACC RCV000045837.2,