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rs397509032

From SNPedia

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


Make rs397509032(-;-)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092541
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509032
dbSNP (old)rs397509032
ClinGenrs397509032
ebirs397509032
HLIrs397509032
Exacrs397509032
Varsomers397509032
Maprs397509032
PheGenIrs397509032
Biobankrs397509032
1000 genomesrs397509032
hgdprs397509032
ensemblrs397509032
gopubmedrs397509032
geneviewrs397509032
scholarrs397509032
googlers397509032
pharmgkbrs397509032
gwascentralrs397509032
openSNPrs397509032
23andMers397509032
23andMe allrs397509032
SNP Nexus

SNPshotrs397509032
SNPdbers397509032
MSV3drs397509032
GWAS Ctlgrs397509032
Max Magnitude6
ClinVar
Risk rs397509032(-;-)
Alt rs397509032(-;-)
Reference Rs397509032(A;A)
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.41244558delT
CLNSRC ClinVar
CLNACC RCV000048031.2, RCV000256846.2,