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rs397509082

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397509082(-;-)
Make rs397509082(-;AA)
Make rs397509082(AA;AA)
ReferenceGRCh38 38.1/141
Chromosome17
Position43091955
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509082
ebirs397509082
HLIrs397509082
Exacrs397509082
Varsomers397509082
Maprs397509082
PheGenIrs397509082
hapmaprs397509082
1000 genomesrs397509082
hgdprs397509082
ensemblrs397509082
gopubmedrs397509082
geneviewrs397509082
scholarrs397509082
googlers397509082
pharmgkbrs397509082
gwascentralrs397509082
openSNPrs397509082
23andMers397509082
23andMe allrs397509082
SNP Nexus

SNPshotrs397509082
SNPdbers397509082
MSV3drs397509082
GWAS Ctlgrs397509082
Max Magnitude0
ClinVar
Risk rs397509082(AA;AA)
Alt rs397509082(AA;AA)
Reference rs397509082(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41243972_41243973insTT
CLNSRC ClinVar
CLNACC RCV000048235.2,