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rs397509080

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CG;CG) 0 common in clinvar
Make rs397509080(-;-)
Make rs397509080(-;CG)
ReferenceGRCh38 38.1/141
Chromosome17
Position43091990
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509080
ebirs397509080
HLIrs397509080
Exacrs397509080
Varsomers397509080
Maprs397509080
PheGenIrs397509080
hapmaprs397509080
1000 genomesrs397509080
hgdprs397509080
ensemblrs397509080
gopubmedrs397509080
geneviewrs397509080
scholarrs397509080
googlers397509080
pharmgkbrs397509080
gwascentralrs397509080
openSNPrs397509080
23andMers397509080
23andMe allrs397509080
SNP Nexus

SNPshotrs397509080
SNPdbers397509080
MSV3drs397509080
GWAS Ctlgrs397509080
Max Magnitude0
ClinVar
Risk rs397509080(;)
Alt rs397509080(;)
Reference rs397509080(CG;CG)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41244007_41244008delCG
CLNSRC ClinVar
CLNACC RCV000048225.2,