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rs1449263

From SNPedia

Orientationminus
Stabilizedminus
Make rs1449263(A;A)
Make rs1449263(A;G)
Make rs1449263(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position181454574
is asnp
is mentioned by
dbSNPrs1449263
ebirs1449263
HLIrs1449263
Exacrs1449263
Varsomers1449263
Maprs1449263
PheGenIrs1449263
hapmaprs1449263
1000 genomesrs1449263
hgdprs1449263
ensemblrs1449263
gopubmedrs1449263
geneviewrs1449263
scholarrs1449263
googlers1449263
pharmgkbrs1449263
gwascentralrs1449263
openSNPrs1449263
23andMers1449263
23andMe allrs1449263
SNP Nexus

SNPshotrs1449263
SNPdbers1449263
MSV3drs1449263
GWAS Ctlgrs1449263
GMAF0.4816
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 19259978] Association of the alpha4 integrin subunit gene (ITGA4) with autism


[PMID 17689671] ITGA4 polymorphisms and susceptibility to multiple sclerosis.

GWAS snp
PMID [PMID 21738480OA-icon.png]
Trait White blood cell count
Title Multiple loci are associated with white blood cell phenotypes.
Risk Allele T
P-val 3E-23
Odds Ratio .04 [0.029-0.044] unit increase