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rs1323292

From SNPedia

Orientationminus
Stabilizedminus
Make rs1323292(C;C)
Make rs1323292(C;T)
Make rs1323292(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position192571891
is asnp
is mentioned by
dbSNPrs1323292
ebirs1323292
HLIrs1323292
Exacrs1323292
Varsomers1323292
Maprs1323292
PheGenIrs1323292
hapmaprs1323292
1000 genomesrs1323292
hgdprs1323292
ensemblrs1323292
gopubmedrs1323292
geneviewrs1323292
scholarrs1323292
googlers1323292
pharmgkbrs1323292
gwascentralrs1323292
openSNPrs1323292
23andMers1323292
23andMe allrs1323292
SNP Nexus

SNPshotrs1323292
SNPdbers1323292
MSV3drs1323292
GWAS Ctlgrs1323292
GMAF0.168
Max Magnitude
? (C;C) (C;T) (T;T) 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 A
P-val 2E-8
Odds Ratio 1.12 [1.1-1.14]