{{Rsnum
|rsid=133885
|Gene=MYO18B
|Chromosome=22
|position=25763322
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=A
|GMAF=0.3186
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=MYO18B
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 18.6 | 54.9 | 26.5
| HCB | 75.9 | 21.9 | 2.2
| JPT | 65.5 | 32.7 | 1.8
| YRI | 78.2 | 21.1 | 0.7
| ASW | 82.5 | 17.5 | 0.0
| CHB | 75.9 | 21.9 | 2.2
| CHD | 69.7 | 25.7 | 4.6
| GIH | 30.7 | 52.5 | 16.8
| LWK | 81.8 | 17.3 | 0.9
| MEX | 53.4 | 41.4 | 5.2
| MKK | 73.7 | 25.6 | 0.6
| TSI | 22.5 | 45.1 | 32.4
| HapMapRevision=28
}}{{Venter SNP
|rsid=133885
|allele=A
|frequency=0.458
|uid=1103691019299
|type=heterozygous_SNP
|hugo=MYO18B
|ensembl gene=ENSG00000133454
|ensembl transcript=ENST00000335473
|sift=
|disease=Defects in MYO18B are associated with lung cancer. Inactivated in half of the primary lung cancers and cell lines; the causes include deletions, mutations and promoter methylation.
}}

{{GET Evidence
|gene=MYO18B
|aa_change=Gly44Glu
|aa_change_short=G44E
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs133885
|overall_frequency_n=5618
|overall_frequency_d=9770
|overall_frequency=0.575026
|n_genomes=47
|n_genomes_annotated=0
|n_haplomes=73
|n_articles=0
|n_articles_annotated=0
|nblosum100=6
|autoscore=0
|webscore=N
}}

{{PMID Auto GWAS
  |PMID=23423138
  |Trait=Mathematical ability in children with dyslexia
  |Title=A common variant in Myosin-18B contributes to mathematical abilities in children with dyslexia and intraparietal sulcus variability in adults.
  |RiskAllele=
  |Pval=8E-10
  |OR=4.87
  |ORtxt=% increase
  |OA=1
}}

{{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}}