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rs397509013

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TAAG;TAAG) 0 common in clinvar
Make rs397509013(-;-)
Make rs397509013(-;TAAG)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092720
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509013
ClinGenrs397509013
ebirs397509013
HLIrs397509013
Exacrs397509013
Varsomers397509013
Maprs397509013
PheGenIrs397509013
hapmaprs397509013
1000 genomesrs397509013
hgdprs397509013
ensemblrs397509013
gopubmedrs397509013
geneviewrs397509013
scholarrs397509013
googlers397509013
pharmgkbrs397509013
gwascentralrs397509013
openSNPrs397509013
23andMers397509013
23andMe allrs397509013
SNP Nexus

SNPshotrs397509013
SNPdbers397509013
MSV3drs397509013
GWAS Ctlgrs397509013
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs397509013(TAAG;TAAG)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41244737_41244740delCTTA
CLNSRC ClinVar
CLNACC RCV000047976.2, RCV000257883.2,