{{Rsnum
|rsid=874628
|Gene=MPV17L2
|Chromosome=19
|position=18193890
|Orientation=minus
|GMAF=0.1919
|Gene_s=MPV17L2
|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 | 6.2 | 44.2 | 49.6
| HCB | 0.7 | 13.9 | 85.4
| JPT | 0.9 | 12.4 | 86.7
| YRI | 2.7 | 34.7 | 62.6
| ASW | 0.0 | 22.8 | 77.2
| CHB | 0.7 | 13.9 | 85.4
| CHD | 2.8 | 21.1 | 76.1
| GIH | 0.0 | 36.6 | 63.4
| LWK | 5.5 | 38.2 | 56.4
| MEX | 6.9 | 24.1 | 69.0
| MKK | 7.1 | 44.2 | 48.7
| TSI | 6.9 | 47.1 | 46.1
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21833088
|Trait=None
|Title=Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
|RiskAllele=A
|Pval=1E-8
|OR=1.1100
|ORtxt=[1.09-1.12]
|OA=1
}}

{{PMID Auto
|PMID=15752431
|Title=Association between a variation in the phosphodiesterase 4D gene and bone mineral density.
|OA=1
}}

{{PMID Auto
|PMID=16584842
|Title=Variants in the RAB3A gene are not associated with mental retardation in the Chinese population.
}}

{{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
|gene=MPV17L2
|aa_change=Met72Val
|aa_change_short=M72V
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs874628
|overall_frequency_n=2521
|overall_frequency_d=10222
|overall_frequency=0.246625
|n_genomes=20
|n_genomes_annotated=0
|n_haplomes=24
|n_articles=0
|n_articles_annotated=0
|pph2_score=0.328
|nblosum100=0
|autoscore=0
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}