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rs397509280

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397509280(A;G)
Make rs397509280(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43049114
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509280
ebirs397509280
HLIrs397509280
Exacrs397509280
Varsomers397509280
Maprs397509280
PheGenIrs397509280
hapmaprs397509280
1000 genomesrs397509280
hgdprs397509280
ensemblrs397509280
gopubmedrs397509280
geneviewrs397509280
scholarrs397509280
googlers397509280
pharmgkbrs397509280
gwascentralrs397509280
openSNPrs397509280
23andMers397509280
23andMe allrs397509280
SNP Nexus

SNPshotrs397509280
SNPdbers397509280
MSV3drs397509280
GWAS Ctlgrs397509280
Max Magnitude0
ClinVar
Risk rs397509280(G;G)
Alt rs397509280(G;G)
Reference rs397509280(A;A)
Significance Probable-non-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.41201131T>C
CLNSRC ClinVar
CLNACC RCV000048979.2, RCV000077622.3,