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rs397509133

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GAAAA;GAAAA) 0 common in clinvar
Make rs397509133(-;-)
Make rs397509133(-;GAAAA)
ReferenceGRCh38 38.1/141
Chromosome17
Position43091470
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509133
ebirs397509133
HLIrs397509133
Exacrs397509133
Varsomers397509133
Maprs397509133
PheGenIrs397509133
hapmaprs397509133
1000 genomesrs397509133
hgdprs397509133
ensemblrs397509133
gopubmedrs397509133
geneviewrs397509133
scholarrs397509133
googlers397509133
pharmgkbrs397509133
gwascentralrs397509133
openSNPrs397509133
23andMers397509133
23andMe allrs397509133
SNP Nexus

SNPshotrs397509133
SNPdbers397509133
MSV3drs397509133
GWAS Ctlgrs397509133
Max Magnitude0
ClinVar
Risk rs397509133(;)
Alt rs397509133(;)
Reference rs397509133(GAAAA;GAAAA)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41243487_41243491delTTTTC
CLNSRC ClinVar
CLNACC RCV000048428.2,