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rs397509137

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs397509137(-;-)
Make rs397509137(-;CT)
ReferenceGRCh38 38.1/141
Chromosome17
Position43091438
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509137
ebirs397509137
HLIrs397509137
Exacrs397509137
Varsomers397509137
Maprs397509137
PheGenIrs397509137
hapmaprs397509137
1000 genomesrs397509137
hgdprs397509137
ensemblrs397509137
gopubmedrs397509137
geneviewrs397509137
scholarrs397509137
googlers397509137
pharmgkbrs397509137
gwascentralrs397509137
openSNPrs397509137
23andMers397509137
23andMe allrs397509137
SNP Nexus

SNPshotrs397509137
SNPdbers397509137
MSV3drs397509137
GWAS Ctlgrs397509137
Max Magnitude0
ClinVar
Risk rs397509137(;)
Alt rs397509137(;)
Reference rs397509137(CT;CT)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41243455_41243456delAG
CLNSRC ClinVar
CLNACC RCV000048439.2,