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rs397508913

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508913(-;-)
Make rs397508913(-;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position43093700
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508913
ebirs397508913
HLIrs397508913
Exacrs397508913
Varsomers397508913
Maprs397508913
PheGenIrs397508913
hapmaprs397508913
1000 genomesrs397508913
hgdprs397508913
ensemblrs397508913
gopubmedrs397508913
geneviewrs397508913
scholarrs397508913
googlers397508913
pharmgkbrs397508913
gwascentralrs397508913
openSNPrs397508913
23andMers397508913
23andMe allrs397508913
SNP Nexus

SNPshotrs397508913
SNPdbers397508913
MSV3drs397508913
GWAS Ctlgrs397508913
Max Magnitude0
ClinVar
Risk rs397508913(;)
Alt rs397508913(;)
Reference rs397508913(C;C)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41245717delG
CLNSRC ClinVar
CLNACC RCV000047604.2,