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rs2744148

From SNPedia

Orientationplus
Stabilizedplus
Make rs2744148(A;A)
Make rs2744148(A;G)
Make rs2744148(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position1023552
is asnp
is mentioned by
dbSNPrs2744148
ebirs2744148
HLIrs2744148
Exacrs2744148
Varsomers2744148
Maprs2744148
PheGenIrs2744148
hapmaprs2744148
1000 genomesrs2744148
hgdprs2744148
ensemblrs2744148
gopubmedrs2744148
geneviewrs2744148
scholarrs2744148
googlers2744148
pharmgkbrs2744148
gwascentralrs2744148
openSNPrs2744148
23andMers2744148
23andMe allrs2744148
SNP Nexus

SNPshotrs2744148
SNPdbers2744148
MSV3drs2744148
GWAS Ctlgrs2744148
GMAF0.1024
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21833088OA-icon.png]
Trait
Title Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
Risk Allele G
P-val 8E-8
Odds Ratio 1.1200 [1.10-1.14]


[PMID 23739915OA-icon.png] MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loci for multiple sclerosis