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rs397508840

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508840(C;T)
Make rs397508840(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094393
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508840
ebirs397508840
HLIrs397508840
Exacrs397508840
Varsomers397508840
Maprs397508840
PheGenIrs397508840
hapmaprs397508840
1000 genomesrs397508840
hgdprs397508840
ensemblrs397508840
gopubmedrs397508840
geneviewrs397508840
scholarrs397508840
googlers397508840
pharmgkbrs397508840
gwascentralrs397508840
openSNPrs397508840
23andMers397508840
23andMe allrs397508840
SNP Nexus

SNPshotrs397508840
SNPdbers397508840
MSV3drs397508840
GWAS Ctlgrs397508840
Max Magnitude0
ClinVar
Risk rs397508840(T;T)
Alt rs397508840(T;T)
Reference rs397508840(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.41246410G>A
CLNSRC ClinVar
CLNACC RCV000047358.2,