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rs397509291

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397509291(-;-)
Make rs397509291(-;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position43045767
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509291
ebirs397509291
HLIrs397509291
Exacrs397509291
Varsomers397509291
Maprs397509291
PheGenIrs397509291
hapmaprs397509291
1000 genomesrs397509291
hgdprs397509291
ensemblrs397509291
gopubmedrs397509291
geneviewrs397509291
scholarrs397509291
googlers397509291
pharmgkbrs397509291
gwascentralrs397509291
openSNPrs397509291
23andMers397509291
23andMe allrs397509291
SNP Nexus

SNPshotrs397509291
SNPdbers397509291
MSV3drs397509291
GWAS Ctlgrs397509291
Max Magnitude0
ClinVar
Risk rs397509291(;)
Alt rs397509291(;)
Reference rs397509291(C;C)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41197784delG
CLNSRC ClinVar
CLNACC RCV000049022.2,