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rs7578982

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;T) 0 common in complete genomics
Make rs7578982(C;C)
Make rs7578982(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position111078961
GeneACOXL
is asnp
is mentioned by
dbSNPrs7578982
ebirs7578982
HLIrs7578982
Exacrs7578982
Varsomers7578982
Maprs7578982
PheGenIrs7578982
hapmaprs7578982
1000 genomesrs7578982
hgdprs7578982
ensemblrs7578982
gopubmedrs7578982
geneviewrs7578982
scholarrs7578982
googlers7578982
pharmgkbrs7578982
gwascentralrs7578982
openSNPrs7578982
23andMers7578982
23andMe allrs7578982
SNP Nexus

SNPshotrs7578982
SNPdbers7578982
MSV3drs7578982
GWAS Ctlgrs7578982
GMAF0.3044
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21738478OA-icon.png]
Trait
Title Identification of nine novel Loci associated with white blood cell subtypes in a Japanese population.
Risk Allele T
P-val 4E-7
Odds Ratio 0.0540 [0.03-0.07] unit increase