Gene entry
MYO5B
myosin VB
- Chromosome
- 18
- Cytoband
- 18q21.1
- Variants (rsID)
- 107
MYO5B is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 18 (region 18q21.1). Its official name is “myosin VB”. The reference table lists 107 variants (rsID) for this gene.
Clinically classified variants
9 reference-table entries with clinical significance.
- rs11082795Benignsingle nucleotide variantCongenital microvillous atrophy
- rs189027956Benignsingle nucleotide variantCongenital microvillous atrophy
- rs1942418Benignsingle nucleotide variantCongenital microvillous atrophy
- rs2298624Benignsingle nucleotide variantCongenital microvillous atrophy
- rs78626055Benignsingle nucleotide variantCongenital microvillous atrophy
- rs79714279Benignsingle nucleotide variantCongenital microvillous atrophy
- rs183277668Uncertain significancesingle nucleotide variantCongenital microvillous atrophy
- rs202205346Uncertain significancesingle nucleotide variantCongenital microvillous atrophy
- rs76213287Uncertain significancesingle nucleotide variantCongenital microvillous atrophy
Other listed variants
- rs506696
- rs533846
- rs616343
- rs630665
- rs1217632
- rs1511150
- rs1511153
- rs1623231
- rs1705520
- rs1705544
- rs1787291
- rs1787296
- rs1787321
- rs1787523
- rs1787557
- rs1790414
- rs1790800
- rs1815937
- rs1893441
- rs1893452
- rs1942416
- rs2000900
- rs2338686
- rs2457965
- rs2469478
- rs2469480
- rs4398183
- rs4513197
- rs4939926
- rs4939928
- rs4939941
- rs6507957
- rs7227820
- rs7235513
- rs7239105
- rs8085876
- rs8086557
- rs8088632
- rs8089039
- rs9304394
- rs9949017
- rs11082803
- rs11659301
- rs11873518
- rs12607902
- rs12959341
- rs12965607
- rs16951195
- rs16951323
- rs17659034
- rs17715292
- rs17716461
- rs17726969
- rs17729191
- rs17801411
- rs17801939
- rs17802336
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.