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rs397509268

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397509268(G;T)
Make rs397509268(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43049186
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509268
ebirs397509268
HLIrs397509268
Exacrs397509268
Varsomers397509268
Maprs397509268
PheGenIrs397509268
hapmaprs397509268
1000 genomesrs397509268
hgdprs397509268
ensemblrs397509268
gopubmedrs397509268
geneviewrs397509268
scholarrs397509268
googlers397509268
pharmgkbrs397509268
gwascentralrs397509268
openSNPrs397509268
23andMers397509268
23andMe allrs397509268
SNP Nexus

SNPshotrs397509268
SNPdbers397509268
MSV3drs397509268
GWAS Ctlgrs397509268
Max Magnitude0
ClinVar
Risk rs397509268(T;T)
Alt rs397509268(T;T)
Reference rs397509268(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.41201203C>A
CLNSRC ClinVar
CLNACC RCV000048949.2, RCV000083220.2,