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rs7018475

From SNPedia

Orientationplus
Stabilizedplus
Make rs7018475(G;G)
Make rs7018475(G;T)
Make rs7018475(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position22137686
is asnp
is mentioned by
dbSNPrs7018475
ebirs7018475
HLIrs7018475
Exacrs7018475
Varsomers7018475
Maprs7018475
PheGenIrs7018475
hapmaprs7018475
1000 genomesrs7018475
hgdprs7018475
ensemblrs7018475
gopubmedrs7018475
geneviewrs7018475
scholarrs7018475
googlers7018475
pharmgkbrs7018475
gwascentralrs7018475
openSNPrs7018475
23andMers7018475
23andMe allrs7018475
SNP Nexus

SNPshotrs7018475
SNPdbers7018475
MSV3drs7018475
GWAS Ctlgrs7018475
GMAF0.2984
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 22293688OA-icon.png]
Trait
Title 1000 Genomes-based imputation identifies novel and refined associations for the Wellcome Trust Case Control Consortium phase 1 Data.
Risk Allele
P-val 3E-8
Odds Ratio 1.3500 None