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rs397509259

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397509259(-;-)
Make rs397509259(-;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43051085
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509259
ebirs397509259
HLIrs397509259
Exacrs397509259
Varsomers397509259
Maprs397509259
PheGenIrs397509259
hapmaprs397509259
1000 genomesrs397509259
hgdprs397509259
ensemblrs397509259
gopubmedrs397509259
geneviewrs397509259
scholarrs397509259
googlers397509259
pharmgkbrs397509259
gwascentralrs397509259
openSNPrs397509259
23andMers397509259
23andMe allrs397509259
SNP Nexus

SNPshotrs397509259
SNPdbers397509259
MSV3drs397509259
GWAS Ctlgrs397509259
Max Magnitude0
ClinVar
Risk rs397509259(;)
Alt rs397509259(;)
Reference rs397509259(G;G)
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.41203102delC
CLNSRC Breast Cancer Information Core (BRCA1)
CLNACC RCV000048920.2, RCV000112606.2,