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rs397509274

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397509274(A;T)
Make rs397509274(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43049150
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509274
ebirs397509274
HLIrs397509274
Exacrs397509274
Varsomers397509274
Maprs397509274
PheGenIrs397509274
hapmaprs397509274
1000 genomesrs397509274
hgdprs397509274
ensemblrs397509274
gopubmedrs397509274
geneviewrs397509274
scholarrs397509274
googlers397509274
pharmgkbrs397509274
gwascentralrs397509274
openSNPrs397509274
23andMers397509274
23andMe allrs397509274
SNP Nexus

SNPshotrs397509274
SNPdbers397509274
MSV3drs397509274
GWAS Ctlgrs397509274
Max Magnitude0
ClinVar
Risk rs397509274(T;T)
Alt rs397509274(T;T)
Reference rs397509274(A;A)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41201167T>A
CLNSRC ClinVar
CLNACC RCV000048967.2,