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rs397509140

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397509140(A;A)
Make rs397509140(A;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43091013
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509140
ebirs397509140
HLIrs397509140
Exacrs397509140
Varsomers397509140
Maprs397509140
PheGenIrs397509140
hapmaprs397509140
1000 genomesrs397509140
hgdprs397509140
ensemblrs397509140
gopubmedrs397509140
geneviewrs397509140
scholarrs397509140
googlers397509140
pharmgkbrs397509140
gwascentralrs397509140
openSNPrs397509140
23andMers397509140
23andMe allrs397509140
SNP Nexus

SNPshotrs397509140
SNPdbers397509140
MSV3drs397509140
GWAS Ctlgrs397509140
Max Magnitude0
ClinVar
Risk rs397509140(A;A)
Alt rs397509140(A;A)
Reference rs397509140(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.41243030A>T
CLNSRC ClinVar
CLNACC RCV000048447.2,