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rs397509331

From SNPedia

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


Make rs397509331(A;A)
ReferenceGRCh38 38.1/141
Chromosome17
Position43115771
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509331
dbSNP (old)rs397509331
ClinGenrs397509331
ebirs397509331
HLIrs397509331
Exacrs397509331
Varsomers397509331
Maprs397509331
PheGenIrs397509331
Biobankrs397509331
1000 genomesrs397509331
hgdprs397509331
ensemblrs397509331
gopubmedrs397509331
geneviewrs397509331
scholarrs397509331
googlers397509331
pharmgkbrs397509331
gwascentralrs397509331
openSNPrs397509331
23andMers397509331
23andMe allrs397509331
SNP Nexus

SNPshotrs397509331
SNPdbers397509331
MSV3drs397509331
GWAS Ctlgrs397509331
Max Magnitude6
ClinVar
Risk rs397509331(A;A)
Alt rs397509331(A;A)
Reference Rs397509331(T;T)
Significance Pathogenic
Disease Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41267788A>T
CLNSRC ClinVar
CLNACC RCV000049180.3, RCV000239109.2,