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rs397509017

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AGGCTCTAGG;AGGCTCTAGG) 0 common in clinvar
Make rs397509017(-;-)
Make rs397509017(-;AGGCTCTAGG)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092678
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509017
ebirs397509017
HLIrs397509017
Exacrs397509017
Varsomers397509017
Maprs397509017
PheGenIrs397509017
hapmaprs397509017
1000 genomesrs397509017
hgdprs397509017
ensemblrs397509017
gopubmedrs397509017
geneviewrs397509017
scholarrs397509017
googlers397509017
pharmgkbrs397509017
gwascentralrs397509017
openSNPrs397509017
23andMers397509017
23andMe allrs397509017
SNP Nexus

SNPshotrs397509017
SNPdbers397509017
MSV3drs397509017
GWAS Ctlgrs397509017
Max Magnitude0
ClinVar
Risk rs397509017(;)
Alt rs397509017(;)
Reference rs397509017(AGGCTCTAGG;AGGCTCTAGG)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41244695_41244704delCCTAGAGCCT
CLNSRC ClinVar
CLNACC RCV000047989.2,