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rs397509103

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;AA) 6 BRCA1 variant considered pathogenic for breast cancer
(AA;AA) 0 common in clinvar


Make rs397509103(-;-)
ReferenceGRCh38 38.1/141
Chromosome17
Position43091767
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509103
dbSNP (old)rs397509103
ClinGenrs397509103
ebirs397509103
HLIrs397509103
Exacrs397509103
Gnomadrs397509103
Varsomers397509103
Maprs397509103
PheGenIrs397509103
Biobankrs397509103
1000 genomesrs397509103
hgdprs397509103
ensemblrs397509103
gopubmedrs397509103
geneviewrs397509103
scholarrs397509103
googlers397509103
pharmgkbrs397509103
gwascentralrs397509103
openSNPrs397509103
23andMers397509103
23andMe allrs397509103
SNP Nexus

SNPshotrs397509103
SNPdbers397509103
MSV3drs397509103
GWAS Ctlgrs397509103
Max Magnitude6
ClinVar
Risk rs397509103(-;-)
Alt rs397509103(-;-)
Reference Rs397509103(AA;AA)
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.41243784_41243785delTT
CLNSRC ClinVar
CLNACC RCV000048323.2, RCV000257218.1,