{{Rsnum
|rsid=6074022
|Chromosome=20
|position=46111557
|Orientation=plus
|GMAF=0.2489
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 3.5 | 40.7 | 55.8
| HCB | 11.7 | 42.3 | 46.0
| JPT | 19.5 | 51.3 | 29.2
| YRI | 0.0 | 1.4 | 98.6
| ASW | 0.0 | 3.5 | 96.5
| CHB | 11.7 | 42.3 | 46.0
| CHD | 15.6 | 40.4 | 44.0
| GIH | 6.9 | 39.6 | 53.5
| LWK | 0.0 | 5.5 | 94.5
| MEX | 6.9 | 39.7 | 53.4
| MKK | 0.6 | 12.2 | 87.2
| TSI | 2.0 | 55.9 | 42.2
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=19525955
|Trait=Multiple sclerosis
|Title=Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20
|RiskAllele=G
|Pval=1E-7
|OR=1.20
|ORtxt=[NR]
}}

{{omim
|id=126200
|rsnum=6074022
}}

{{PMID Auto GWAS
|PMID=22190364
|Trait=None
|Title=Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci.
|RiskAllele=C
|Pval=0.000005
|OR=1.1500
|ORtxt=None
|OA=1
}}

{{PMID Auto
|PMID=20368992
|Title=Multiple sclerosis susceptibility-associated SNPs do not influence disease severity measures in a cohort of Australian MS patients.
|OA=1
}}

{{PMID Auto
|PMID=20405052
|Title=The effect of single nucleotide polymorphisms from genome wide association studies in multiple sclerosis on gene expression.
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs6074022
|overall_frequency_n=101
|overall_frequency_d=128
|overall_frequency=0.789062
|n_genomes=51
|n_genomes_annotated=0
|n_haplomes=91
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

{{PMID Auto
|PMID=23613777
|Title=Association of SNPs of CD40 gene with multiple sclerosis in Russians.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}