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rs397509289

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397509289(-;-)
Make rs397509289(-;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43097289
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509289
ebirs397509289
HLIrs397509289
Exacrs397509289
Varsomers397509289
Maprs397509289
PheGenIrs397509289
hapmaprs397509289
1000 genomesrs397509289
hgdprs397509289
ensemblrs397509289
gopubmedrs397509289
geneviewrs397509289
scholarrs397509289
googlers397509289
pharmgkbrs397509289
gwascentralrs397509289
openSNPrs397509289
23andMers397509289
23andMe allrs397509289
SNP Nexus

SNPshotrs397509289
SNPdbers397509289
MSV3drs397509289
GWAS Ctlgrs397509289
Max Magnitude0
ClinVar
Risk rs397509289(;)
Alt rs397509289(;)
Reference rs397509289(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.41249306delC
CLNSRC ClinVar
CLNACC RCV000049014.2,