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rs9259013

From SNPedia

Orientationplus
Stabilizedplus
Make rs9259013(A;A)
Make rs9259013(A;T)
Make rs9259013(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position29874690
is asnp
is mentioned by
dbSNPrs9259013
dbSNP (classic)rs9259013
ClinGenrs9259013
ebirs9259013
HLIrs9259013
Exacrs9259013
Gnomadrs9259013
Varsomers9259013
LitVarrs9259013
Maprs9259013
PheGenIrs9259013
Biobankrs9259013
1000 genomesrs9259013
hgdprs9259013
ensemblrs9259013
geneviewrs9259013
scholarrs9259013
googlers9259013
pharmgkbrs9259013
gwascentralrs9259013
openSNPrs9259013
23andMers9259013
23andMe allrs9259013
SNPshotrs9259013
SNPdbers9259013
MSV3drs9259013
GWAS Ctlgrs9259013
Merged fromRs112166594
Max Magnitude0

Formerly known as rs112166594 and associated with Behçet's disease [PMID 24821759OA-icon.png]