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rs397509090

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397509090(-;-)
Make rs397509090(-;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43091903
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509090
ebirs397509090
HLIrs397509090
Exacrs397509090
Varsomers397509090
Maprs397509090
PheGenIrs397509090
hapmaprs397509090
1000 genomesrs397509090
hgdprs397509090
ensemblrs397509090
gopubmedrs397509090
geneviewrs397509090
scholarrs397509090
googlers397509090
pharmgkbrs397509090
gwascentralrs397509090
openSNPrs397509090
23andMers397509090
23andMe allrs397509090
SNP Nexus

SNPshotrs397509090
SNPdbers397509090
MSV3drs397509090
GWAS Ctlgrs397509090
Max Magnitude0
ClinVar
Risk rs397509090(;)
Alt rs397509090(;)
Reference rs397509090(G;G)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41243920delC
CLNSRC ClinVar
CLNACC RCV000048264.2,