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rs17282391

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs17282391(A;G)
Make rs17282391(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position46137989
is asnp
is mentioned by
dbSNPrs17282391
ebirs17282391
HLIrs17282391
Exacrs17282391
Varsomers17282391
Maprs17282391
PheGenIrs17282391
hapmaprs17282391
1000 genomesrs17282391
hgdprs17282391
ensemblrs17282391
gopubmedrs17282391
geneviewrs17282391
scholarrs17282391
googlers17282391
pharmgkbrs17282391
gwascentralrs17282391
openSNPrs17282391
23andMers17282391
23andMe allrs17282391
SNP Nexus

SNPshotrs17282391
SNPdbers17282391
MSV3drs17282391
GWAS Ctlgrs17282391
GMAF0.05923
Max Magnitude0
? (A;A) (A;G) (G;G) 28

[PMID 22829007] Two-stage association study in Chinese Han identifies two independent associations in CCR1/CCR3 locus as candidate for Behçet's disease susceptibility