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rs397509284

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397509284(A;A)
Make rs397509284(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43047665
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509284
ebirs397509284
HLIrs397509284
Exacrs397509284
Varsomers397509284
Maprs397509284
PheGenIrs397509284
hapmaprs397509284
1000 genomesrs397509284
hgdprs397509284
ensemblrs397509284
gopubmedrs397509284
geneviewrs397509284
scholarrs397509284
googlers397509284
pharmgkbrs397509284
gwascentralrs397509284
openSNPrs397509284
23andMers397509284
23andMe allrs397509284
SNP Nexus

SNPshotrs397509284
SNPdbers397509284
MSV3drs397509284
GWAS Ctlgrs397509284
Max Magnitude0
ClinVar
Risk rs397509284(A;A)
Alt rs397509284(A;A)
Reference rs397509284(G;G)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 1 Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.41199682C>T
CLNSRC ClinVar
CLNACC RCV000048997.2, RCV000077624.2, RCV000166210.1,