{{Rsnum
|rsid=33928909
|Gene=MYO18B
|Chromosome=22
|position=25890771
|Orientation=plus
|ReferenceAllele=T
|MissenseAllele=A
|GMAF=0.0326
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene_s=MYO18B
}}{{Venter SNP
|rsid=33928909
|allele=A
|frequency=
|uid=1103691019590
|type=heterozygous_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=Ser1444Thr
|aa_change_short=S1444T
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs33928909
|overall_frequency_n=361
|overall_frequency_d=10526
|overall_frequency=0.034296
|n_genomes=2
|n_genomes_annotated=0
|n_haplomes=2
|n_articles=0
|n_articles_annotated=0
|nblosum100=-2
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}