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rs2920001

From SNPedia

Orientationplus
Stabilizedplus
Make rs2920001(C;C)
Make rs2920001(C;T)
Make rs2920001(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position31209762
is asnp
is mentioned by
dbSNPrs2920001
ebirs2920001
HLIrs2920001
Exacrs2920001
Varsomers2920001
Maprs2920001
PheGenIrs2920001
hapmaprs2920001
1000 genomesrs2920001
hgdprs2920001
ensemblrs2920001
gopubmedrs2920001
geneviewrs2920001
scholarrs2920001
googlers2920001
pharmgkbrs2920001
gwascentralrs2920001
openSNPrs2920001
23andMers2920001
23andMe allrs2920001
SNP Nexus

SNPshotrs2920001
SNPdbers2920001
MSV3drs2920001
GWAS Ctlgrs2920001
GMAF0.1804
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23412934OA-icon.png]
Trait Multiple sclerosis
Title A genome-wide association study of brain lesion distribution in multiple sclerosis.
Risk Allele
P-val 1E-6
Odds Ratio NR NR