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rs397509110

From SNPedia

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


Make rs397509110(-;-)
ReferenceGRCh38 38.1/141
Chromosome17
Position43091711
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509110
dbSNP (old)rs397509110
ClinGenrs397509110
ebirs397509110
HLIrs397509110
Exacrs397509110
Varsomers397509110
Maprs397509110
PheGenIrs397509110
Biobankrs397509110
1000 genomesrs397509110
hgdprs397509110
ensemblrs397509110
gopubmedrs397509110
geneviewrs397509110
scholarrs397509110
googlers397509110
pharmgkbrs397509110
gwascentralrs397509110
openSNPrs397509110
23andMers397509110
23andMe allrs397509110
SNP Nexus

SNPshotrs397509110
SNPdbers397509110
MSV3drs397509110
GWAS Ctlgrs397509110
Max Magnitude6
ClinVar
Risk rs397509110(-;-)
Alt rs397509110(-;-)
Reference Rs397509110(G;G)
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.41243728delC
CLNSRC ClinVar
CLNACC RCV000048343.2, RCV000256600.2,