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rs397509331

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397509331(A;A)
Make rs397509331(A;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43115771
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509331
ebirs397509331
HLIrs397509331
Exacrs397509331
Varsomers397509331
Maprs397509331
PheGenIrs397509331
hapmaprs397509331
1000 genomesrs397509331
hgdprs397509331
ensemblrs397509331
gopubmedrs397509331
geneviewrs397509331
scholarrs397509331
googlers397509331
pharmgkbrs397509331
gwascentralrs397509331
openSNPrs397509331
23andMers397509331
23andMe allrs397509331
SNP Nexus

SNPshotrs397509331
SNPdbers397509331
MSV3drs397509331
GWAS Ctlgrs397509331
Max Magnitude0
ClinVar
Risk rs397509331(A;A)
Alt rs397509331(A;A)
Reference rs397509331(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.41267788A>T
CLNSRC ClinVar
CLNACC RCV000049180.2, RCV000239109.1,