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rs397508859

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508859(G;G)
Make rs397508859(G;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43106539
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508859
ebirs397508859
HLIrs397508859
Exacrs397508859
Varsomers397508859
Maprs397508859
PheGenIrs397508859
hapmaprs397508859
1000 genomesrs397508859
hgdprs397508859
ensemblrs397508859
gopubmedrs397508859
geneviewrs397508859
scholarrs397508859
googlers397508859
pharmgkbrs397508859
gwascentralrs397508859
openSNPrs397508859
23andMers397508859
23andMe allrs397508859
SNP Nexus

SNPshotrs397508859
SNPdbers397508859
MSV3drs397508859
GWAS Ctlgrs397508859
Max Magnitude0
ClinVar
Risk rs397508859(G;G)
Alt rs397508859(G;G)
Reference rs397508859(T;T)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41258556A>C
CLNSRC ClinVar
CLNACC RCV000047436.2,