{{Rsnum
|rsid=2039485
|Chromosome=14
|position=31884044
|Orientation=plus
|GMAF=0.2576
|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 | 5.4 | 39.3 | 55.4
| HCB | 26.3 | 48.9 | 24.8
| JPT | 19.5 | 54.0 | 26.5
| YRI | 0.7 | 12.9 | 86.4
| ASW | 0.0 | 24.6 | 75.4
| CHB | 26.3 | 48.9 | 24.8
| CHD | 26.9 | 45.4 | 27.8
| GIH | 12.9 | 44.6 | 42.6
| LWK | 0.0 | 8.3 | 91.7
| MEX | 5.2 | 29.3 | 65.5
| MKK | 0.0 | 15.4 | 84.6
| TSI | 3.9 | 34.3 | 61.8
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=19010793
|Trait=Brain lesion load
|Title=Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis
|RiskAllele=
|Pval=0.000006
|OR=NR
|ORtxt=NR
}}

{{PharmGKB
|RSID=rs2039485
|Name_s=
|Gene_s=-
|Feature=
|Evidence=PubMed ID:19010793; Web Resource:http://www.genome.gov/gwastudies/
|Annotation=GWAS results: Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. (Initial Sample Size: 791 cases, 883 controls; Replication Sample Size: NR); (Region: 14q12; Reported Gene(s): NUBPL; Risk Allele: rs2039485-?); (p-value= 0.000006).This variant is associated with Brain lesion load.
|Drugs=
|Drug Classes=
|Diseases=
|Curation Level=Non-Curated
|PharmGKB Accession ID=PA164740338
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2039485
|overall_frequency_n=25
|overall_frequency_d=128
|overall_frequency=0.195312
|n_genomes=18
|n_genomes_annotated=0
|n_haplomes=20
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|in_pharmgkb=Y
|autoscore=2
|webscore=N
}}

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