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rs13075270

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs13075270(C;C)
Make rs13075270(C;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position46212298
is asnp
is mentioned by
dbSNPrs13075270
ebirs13075270
HLIrs13075270
Exacrs13075270
Varsomers13075270
Maprs13075270
PheGenIrs13075270
hapmaprs13075270
1000 genomesrs13075270
hgdprs13075270
ensemblrs13075270
gopubmedrs13075270
geneviewrs13075270
scholarrs13075270
googlers13075270
pharmgkbrs13075270
gwascentralrs13075270
openSNPrs13075270
23andMers13075270
23andMe allrs13075270
SNP Nexus

SNPshotrs13075270
SNPdbers13075270
MSV3drs13075270
GWAS Ctlgrs13075270
GMAF0.1157
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