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rs397509183

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs397509183(-;-)
Make rs397509183(-;AG)
ReferenceGRCh38 38.1/141
Chromosome17
Position43074471
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509183
ebirs397509183
HLIrs397509183
Exacrs397509183
Varsomers397509183
Maprs397509183
PheGenIrs397509183
hapmaprs397509183
1000 genomesrs397509183
hgdprs397509183
ensemblrs397509183
gopubmedrs397509183
geneviewrs397509183
scholarrs397509183
googlers397509183
pharmgkbrs397509183
gwascentralrs397509183
openSNPrs397509183
23andMers397509183
23andMe allrs397509183
SNP Nexus

SNPshotrs397509183
SNPdbers397509183
MSV3drs397509183
GWAS Ctlgrs397509183
Max Magnitude0
ClinVar
Risk rs397509183(;)
Alt rs397509183(;)
Reference rs397509183(AG;AG)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41226488_41226489delCT
CLNSRC ClinVar
CLNACC RCV000048590.2,