Gene entry
MYO18B
myosin XVIIIB
- Chromosome
- 22
- Cytoband
- 22q12.1
- Variants (rsID)
- 123
MYO18B is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 22 (region 22q12.1). Its official name is “myosin XVIIIB”. The reference table lists 123 variants (rsID) for this gene.
Clinically classified variants
5 reference-table entries with clinical significance.
- rs149103381Conflicting interpretationssingle nucleotide variantKlippel-Feil anomaly-myopathy-facial dysmorphism syndrome
- rs133885Not classifiedmissense_variantDyslexia|Dysphasia, Familial Developmental|Dyscalculia|Specific Language Impairment
- rs35578357Not classifiedmissense_variant
- rs5761170Not classifiedmissense_variant
- rs5996988Not classifiedsynonymous_variant
Other listed variants
- rs133860
- rs133902
- rs695427
- rs695430
- rs713734
- rs739281
- rs739282
- rs910521
- rs1013815
- rs1158340
- rs1573755
- rs1894677
- rs2038323
- rs2269638
- rs2301492
- rs2331195
- rs2748221
- rs3887776
- rs4820654
- rs4822669
- rs4822682
- rs5752216
- rs5752254
- rs5752257
- rs5761250
- rs5761271
- rs5761308
- rs5761313
- rs5996973
- rs5996984
- rs5996993
- rs6004758
- rs6004774
- rs6004789
- rs6004840
- rs6004851
- rs6004864
- rs6004913
- rs6004919
- rs7286591
- rs7287110
- rs7288885
- rs7292853
- rs8136102
- rs8138918
- rs8139900
- rs8142661
- rs9306419
- rs9608422
- rs9613037
- rs9620576
- rs9624898
- rs9624909
- rs9624920
- rs9624968
- rs9968038
- rs11090409
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.