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rs397509089

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397509089(-;-)
Make rs397509089(-;T)
Make rs397509089(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43091904
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509089
ebirs397509089
HLIrs397509089
Exacrs397509089
Varsomers397509089
Maprs397509089
PheGenIrs397509089
hapmaprs397509089
1000 genomesrs397509089
hgdprs397509089
ensemblrs397509089
gopubmedrs397509089
geneviewrs397509089
scholarrs397509089
googlers397509089
pharmgkbrs397509089
gwascentralrs397509089
openSNPrs397509089
23andMers397509089
23andMe allrs397509089
SNP Nexus

SNPshotrs397509089
SNPdbers397509089
MSV3drs397509089
GWAS Ctlgrs397509089
Max Magnitude0
ClinVar
Risk rs397509089(T;T)
Alt rs397509089(T;T)
Reference rs397509089(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41243922dupA
CLNSRC ClinVar
CLNACC RCV000048262.2,