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rs397509028

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397509028(-;-)
Make rs397509028(-;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092564
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509028
ebirs397509028
HLIrs397509028
Exacrs397509028
Varsomers397509028
Maprs397509028
PheGenIrs397509028
hapmaprs397509028
1000 genomesrs397509028
hgdprs397509028
ensemblrs397509028
gopubmedrs397509028
geneviewrs397509028
scholarrs397509028
googlers397509028
pharmgkbrs397509028
gwascentralrs397509028
openSNPrs397509028
23andMers397509028
23andMe allrs397509028
SNP Nexus

SNPshotrs397509028
SNPdbers397509028
MSV3drs397509028
GWAS Ctlgrs397509028
Max Magnitude0
ClinVar
Risk rs397509028(;)
Alt rs397509028(;)
Reference rs397509028(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.41244581delA
CLNSRC ClinVar
CLNACC RCV000048025.2,