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rs397509159

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs397509159(-;-)
Make rs397509159(-;AG)
ReferenceGRCh38 38.1/141
Chromosome17
Position43082478
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509159
ebirs397509159
HLIrs397509159
Exacrs397509159
Varsomers397509159
Maprs397509159
PheGenIrs397509159
hapmaprs397509159
1000 genomesrs397509159
hgdprs397509159
ensemblrs397509159
gopubmedrs397509159
geneviewrs397509159
scholarrs397509159
googlers397509159
pharmgkbrs397509159
gwascentralrs397509159
openSNPrs397509159
23andMers397509159
23andMe allrs397509159
SNP Nexus

SNPshotrs397509159
SNPdbers397509159
MSV3drs397509159
GWAS Ctlgrs397509159
Max Magnitude0
ClinVar
Risk rs397509159(;)
Alt rs397509159(;)
Reference rs397509159(AG;AG)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41234495_41234496delCT
CLNSRC ClinVar
CLNACC RCV000048512.2,