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rs397509261

From SNPedia

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


Make rs397509261(-;-)
ReferenceGRCh38 38.1/141
Chromosome17
Position43051080
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509261
ClinGenrs397509261
ebirs397509261
HLIrs397509261
Exacrs397509261
Varsomers397509261
Maprs397509261
PheGenIrs397509261
hapmaprs397509261
1000 genomesrs397509261
hgdprs397509261
ensemblrs397509261
gopubmedrs397509261
geneviewrs397509261
scholarrs397509261
googlers397509261
pharmgkbrs397509261
gwascentralrs397509261
openSNPrs397509261
23andMers397509261
23andMe allrs397509261
SNP Nexus

SNPshotrs397509261
SNPdbers397509261
MSV3drs397509261
GWAS Ctlgrs397509261
Max Magnitude6
ClinVar
Risk rs397509261(-;-)
Alt rs397509261(-;-)
Reference Rs397509261(T;T)
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.41203097delA
CLNSRC ClinVar
CLNACC RCV000048924.2, RCV000257542.1,