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rs397508028

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508028(G;G)
Make rs397508028(G;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32379787
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508028
ebirs397508028
HLIrs397508028
Exacrs397508028
Varsomers397508028
Maprs397508028
PheGenIrs397508028
hapmaprs397508028
1000 genomesrs397508028
hgdprs397508028
ensemblrs397508028
gopubmedrs397508028
geneviewrs397508028
scholarrs397508028
googlers397508028
pharmgkbrs397508028
gwascentralrs397508028
openSNPrs397508028
23andMers397508028
23andMe allrs397508028
SNP Nexus

SNPshotrs397508028
SNPdbers397508028
MSV3drs397508028
GWAS Ctlgrs397508028
Max Magnitude0
ClinVar
Risk rs397508028(G;G)
Alt rs397508028(G;G)
Reference rs397508028(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.32953924T>G
CLNSRC ClinVar
CLNACC RCV000045682.2,