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rs13092160

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs13092160(C;C)
Make rs13092160(C;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position46213300
is asnp
is mentioned by
dbSNPrs13092160
ebirs13092160
HLIrs13092160
Exacrs13092160
Varsomers13092160
Maprs13092160
PheGenIrs13092160
hapmaprs13092160
1000 genomesrs13092160
hgdprs13092160
ensemblrs13092160
gopubmedrs13092160
geneviewrs13092160
scholarrs13092160
googlers13092160
pharmgkbrs13092160
gwascentralrs13092160
openSNPrs13092160
23andMers13092160
23andMe allrs13092160
SNP Nexus

SNPshotrs13092160
SNPdbers13092160
MSV3drs13092160
GWAS Ctlgrs13092160
GMAF0.08907
Max Magnitude0
? (C;C) (C;T) (T;T) 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