{{Rsnum
|rsid=7786877
|Gene=MOSPD3
|Chromosome=7
|position=100616392
|Orientation=plus
|GMAF=0.2025
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 61.8 | 34.5 | 3.6
| HCB | 82.1 | 17.2 | 0.7
| JPT | 83.6 | 16.4 | 0.0
| YRI | 67.1 | 30.8 | 2.1
| ASW | 73.7 | 24.6 | 1.8
| CHB | 82.1 | 17.2 | 0.7
| CHD | 76.1 | 21.1 | 2.8
| GIH | 56.6 | 37.4 | 6.1
| LWK | 65.5 | 31.8 | 2.7
| MEX | 56.1 | 36.8 | 7.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 52.0 | 42.0 | 6.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=19862010
|Trait=Mean corpuscular volume
|Title=Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium
|RiskAllele=G
|Pval=3E-11
|OR=0
|ORtxt=[0.002-0.004] fl increase
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs7786877
|overall_frequency_n=31
|overall_frequency_d=128
|overall_frequency=0.242188
|n_genomes=25
|n_genomes_annotated=0
|n_haplomes=29
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

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