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rs397509260

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397509260(-;-)
Make rs397509260(-;G)
Make rs397509260(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43051084
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509260
ebirs397509260
HLIrs397509260
Exacrs397509260
Varsomers397509260
Maprs397509260
PheGenIrs397509260
hapmaprs397509260
1000 genomesrs397509260
hgdprs397509260
ensemblrs397509260
gopubmedrs397509260
geneviewrs397509260
scholarrs397509260
googlers397509260
pharmgkbrs397509260
gwascentralrs397509260
openSNPrs397509260
23andMers397509260
23andMe allrs397509260
SNP Nexus

SNPshotrs397509260
SNPdbers397509260
MSV3drs397509260
GWAS Ctlgrs397509260
Max Magnitude0
ClinVar
Risk rs397509260(G;G)
Alt rs397509260(G;G)
Reference rs397509260(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41203102dupC
CLNSRC ClinVar
CLNACC RCV000048921.2,