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rs397509144

From SNPedia

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


Make rs397509144(-;-)
ReferenceGRCh38 38.1/141
Chromosome17
Position43090961
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509144
ClinGenrs397509144
ebirs397509144
HLIrs397509144
Exacrs397509144
Varsomers397509144
Maprs397509144
PheGenIrs397509144
hapmaprs397509144
1000 genomesrs397509144
hgdprs397509144
ensemblrs397509144
gopubmedrs397509144
geneviewrs397509144
scholarrs397509144
googlers397509144
pharmgkbrs397509144
gwascentralrs397509144
openSNPrs397509144
23andMers397509144
23andMe allrs397509144
SNP Nexus

SNPshotrs397509144
SNPdbers397509144
MSV3drs397509144
GWAS Ctlgrs397509144
Max Magnitude6
ClinVar
Risk rs397509144(-;-)
Alt rs397509144(-;-)
Reference Rs397509144(TG;TG)
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.41242978_41242979delCA
CLNSRC ClinVar
CLNACC RCV000048466.2, RCV000257153.2,