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rs397509296

From SNPedia

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


Make rs397509296(-;-)
ReferenceGRCh38 38.1/141
Chromosome17
Position43045722
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509296
dbSNP (old)rs397509296
ClinGenrs397509296
ebirs397509296
HLIrs397509296
Exacrs397509296
Gnomadrs397509296
Varsomers397509296
Maprs397509296
PheGenIrs397509296
Biobankrs397509296
1000 genomesrs397509296
hgdprs397509296
ensemblrs397509296
gopubmedrs397509296
geneviewrs397509296
scholarrs397509296
googlers397509296
pharmgkbrs397509296
gwascentralrs397509296
openSNPrs397509296
23andMers397509296
23andMe allrs397509296
SNP Nexus

SNPshotrs397509296
SNPdbers397509296
MSV3drs397509296
GWAS Ctlgrs397509296
Max Magnitude6
ClinVar
Risk rs397509296(-;-)
Alt rs397509296(-;-)
Reference Rs397509296(C;C)
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.41197739delG
CLNSRC ClinVar
CLNACC RCV000049045.2, RCV000257302.2,