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rs4648356

From SNPedia

Orientationplus
Stabilizedplus
Make rs4648356(A;A)
Make rs4648356(A;C)
Make rs4648356(C;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position2792599
is asnp
is mentioned by
dbSNPrs4648356
ebirs4648356
HLIrs4648356
Exacrs4648356
Varsomers4648356
Maprs4648356
PheGenIrs4648356
hapmaprs4648356
1000 genomesrs4648356
hgdprs4648356
ensemblrs4648356
gopubmedrs4648356
geneviewrs4648356
scholarrs4648356
googlers4648356
pharmgkbrs4648356
gwascentralrs4648356
openSNPrs4648356
23andMers4648356
23andMe allrs4648356
SNP Nexus

SNPshotrs4648356
SNPdbers4648356
MSV3drs4648356
GWAS Ctlgrs4648356
GMAF0.4197
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 21833088OA-icon.png]
Trait Multiple sclerosis
Title Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
Risk Allele C
P-val 1E-14
Odds Ratio 1.14 [1.12-1.16]