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rs397509052

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397509052(-;-)
Make rs397509052(-;A)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092242
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509052
ebirs397509052
HLIrs397509052
Exacrs397509052
Varsomers397509052
Maprs397509052
PheGenIrs397509052
hapmaprs397509052
1000 genomesrs397509052
hgdprs397509052
ensemblrs397509052
gopubmedrs397509052
geneviewrs397509052
scholarrs397509052
googlers397509052
pharmgkbrs397509052
gwascentralrs397509052
openSNPrs397509052
23andMers397509052
23andMe allrs397509052
SNP Nexus

SNPshotrs397509052
SNPdbers397509052
MSV3drs397509052
GWAS Ctlgrs397509052
Max Magnitude0
ClinVar
Risk rs397509052(;)
Alt rs397509052(;)
Reference rs397509052(A;A)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41244259delT
CLNSRC ClinVar
CLNACC RCV000048126.2,