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rs397509045

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AGTA;AGTA) 0 common in clinvar
Make rs397509045(-;-)
Make rs397509045(-;AGTA)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092359
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509045
ebirs397509045
HLIrs397509045
Exacrs397509045
Varsomers397509045
Maprs397509045
PheGenIrs397509045
hapmaprs397509045
1000 genomesrs397509045
hgdprs397509045
ensemblrs397509045
gopubmedrs397509045
geneviewrs397509045
scholarrs397509045
googlers397509045
pharmgkbrs397509045
gwascentralrs397509045
openSNPrs397509045
23andMers397509045
23andMe allrs397509045
SNP Nexus

SNPshotrs397509045
SNPdbers397509045
MSV3drs397509045
GWAS Ctlgrs397509045
Max Magnitude0
ClinVar
Risk rs397509045(;)
Alt rs397509045(;)
Reference rs397509045(AGTA;AGTA)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41244376_41244379delTACT
CLNSRC ClinVar
CLNACC RCV000048091.2,