{{Rsnum
|rsid=3859866
|Gene=MYO18B
|Chromosome=22
|position=25770933
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=C
|GMAF=0.05556
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=MYO18B
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 95.6 | 4.4 | 0.0
| HCB | 74.5 | 21.9 | 3.6
| JPT | 78.8 | 17.7 | 3.5
| YRI | 93.2 | 6.1 | 0.7
| ASW | 91.2 | 8.8 | 0.0
| CHB | 74.5 | 21.9 | 3.6
| CHD | 67.0 | 33.0 | 0.0
| GIH | 85.0 | 15.0 | 0.0
| LWK | 89.0 | 10.1 | 0.9
| MEX | 98.3 | 1.7 | 0.0
| MKK | 86.5 | 13.5 | 0.0
| TSI | 98.0 | 2.0 | 0.0
| HapMapRevision=28
}}

{{Venter SNP
|rsid=3859866
|allele=C
|frequency=0.983
|uid=1103691019309
|type=homozygous_SNP
|hugo=MYO18B
|ensembl gene=ENSG00000133454
|ensembl transcript=ENST00000335473
|sift=TOLERATED
|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=Trp547Cys
|aa_change_short=W547C
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs3859866
|overall_frequency_n=9951
|overall_frequency_d=10172
|overall_frequency=0.978274
|n_genomes=55
|n_genomes_annotated=0
|n_haplomes=106
|n_articles=0
|n_articles_annotated=0
|nblosum100=7
|autoscore=0
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}