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rs397508986

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508986(C;TT)
Make rs397508986(TT;TT)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092919
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508986
ebirs397508986
HLIrs397508986
Exacrs397508986
Varsomers397508986
Maprs397508986
PheGenIrs397508986
hapmaprs397508986
1000 genomesrs397508986
hgdprs397508986
ensemblrs397508986
gopubmedrs397508986
geneviewrs397508986
scholarrs397508986
googlers397508986
pharmgkbrs397508986
gwascentralrs397508986
openSNPrs397508986
23andMers397508986
23andMe allrs397508986
SNP Nexus

SNPshotrs397508986
SNPdbers397508986
MSV3drs397508986
GWAS Ctlgrs397508986
Max Magnitude0
ClinVar
Risk rs397508986(TT;TT)
Alt rs397508986(TT;TT)
Reference rs397508986(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.41244936delGinsAA
CLNSRC ClinVar
CLNACC RCV000047901.2,