MYO1H

myosin IH

Summary

Predicted to enable actin filament binding activity and microfilament motor activity. Predicted to be involved in actin filament organization; actin filament-based movement; and endocytosis. Predicted to be part of myosin complex. Predicted to be active in several cellular components, including actin cytoskeleton; microvillus; and plasma membrane. Implicated in congenital central hypoventilation syndrome. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants102 total

rsidPosition (GRCh37)AllelesClassClinVar
rs287905412:109,766,137G/Cintergenic variant—
rs3584504312:109,768,732G/Tintergenic variant—
rs6193648312:109,797,966C/Aupstream gene variant—
rs1106644012:109,813,508A/T——
rs8002836012:109,826,540C/T—likely benign
rs75505849212:109,826,595C/A—uncertain significance
rs77178357412:109,826,626C/T—uncertain significance
rs122775906612:109,826,627G/A—uncertain significance
rs1106647112:109,828,039T/Cintron variant—
rs76820117812:109,831,172T/C—uncertain significance
rs37732897612:109,831,196G/A—uncertain significance
rs730029012:109,832,545T/Gintron variant—
rs76545760212:109,834,208G/A—uncertain significance
rs77405410112:109,834,215G/A—uncertain significance
rs55221367512:109,834,271G/T—uncertain significance
rs74921616612:109,834,287C/T—uncertain significance
rs53474141812:109,834,353G/A—uncertain significance
rs76860055612:109,835,552A/G—uncertain significance
rs20083906712:109,835,556C/T—uncertain significance
rs20179341312:109,835,562G/A—uncertain significance
rs77594583812:109,838,907G/A—uncertain significance
rs20053255112:109,838,926G/T—likely benign
rs90459439212:109,838,944C/A—uncertain significance
rs54822150512:109,838,947G/A—uncertain significance
rs86752351312:109,838,964G/A—uncertain significance
rs77107516412:109,838,995A/C—uncertain significance
rs127205217612:109,839,012G/A—uncertain significance
rs56842416212:109,839,042G/C—uncertain significance
rs994375312:109,840,940A/T——
rs15095910812:109,841,847G/A—uncertain significance
rs6174037112:109,841,854C/G—benign
rs11659704712:109,843,751G/C—uncertain significance
rs94258003012:109,843,772G/A—uncertain significance
rs249995350912:109,843,800C/T—uncertain significance
rs55916330712:109,843,821A/C—uncertain significance
rs249995559512:109,844,615G/A—uncertain significance
rs74561761712:109,845,598G/T—uncertain significance
rs11744252112:109,845,660T/A—benign
rs20142313512:109,845,669G/A—uncertain significance
rs37355508512:109,845,699A/G—uncertain significance
rs77588555912:109,847,384T/C—uncertain significance
rs94804501612:109,847,782G/A—uncertain significance
rs5591384212:109,847,787A/G—uncertain significance
rs148542109212:109,847,789T/A—uncertain significance
rs37227077612:109,848,500C/T—uncertain significance
rs37491618112:109,848,527T/C—uncertain significance
rs37208076012:109,848,553A/G—uncertain significance
rs731648612:109,849,540A/Gintron variant—
rs18396734412:109,849,714C/T—likely benign
rs74653519712:109,849,781A/G—uncertain significance
rs476659812:109,853,306A/T——
rs75059413012:109,853,333G/A—uncertain significance
rs75646718912:109,853,345G/A—uncertain significance
rs74905387812:109,853,348C/T—uncertain significance
rs56727895012:109,853,363G/A—uncertain significance
rs76598084012:109,853,384G/C—uncertain significance
rs6809404712:109,855,201C/Tintron variant—
rs187115261612:109,858,818A/G—uncertain significance
rs75020093612:109,862,569A/G—uncertain significance
rs37279187512:109,862,617G/C—uncertain significance
rs57041371712:109,862,625C/G—uncertain significance
rs75819889712:109,862,631A/G—uncertain significance
rs144476828412:109,863,754G/T—uncertain significance
rs76254454212:109,863,801C/G—uncertain significance
rs36987540712:109,863,806A/G—uncertain significance
rs20166114612:109,863,835C/T—uncertain significance
rs54470384112:109,863,841G/A—uncertain significance
rs37391143212:109,863,853C/T—uncertain significance
rs75159557312:109,865,274G/A—uncertain significance
rs75548430612:109,865,277A/T—uncertain significance
rs75415843012:109,865,387C/G—uncertain significance
rs7786660212:109,866,611T/C——
rs731305612:109,871,458T/Cregulatory region variant—
rs76415015112:109,872,858C/T—uncertain significance
rs1085013712:109,874,794C/A——
rs1085013912:109,875,934A/T——
rs52811545112:109,876,359A/G—uncertain significance
rs19069374112:109,876,365G/A—uncertain significance
rs75739928712:109,876,380G/A—uncertain significance
rs74739679412:109,876,413G/A—likely benign
rs37502673712:109,877,459G/T—uncertain significance
rs144669558012:109,877,462A/T—uncertain significance
rs7452815512:109,877,506C/T—benign
rs118531842812:109,877,554C/G—uncertain significance
rs18758255412:109,877,575C/T—uncertain significance
rs77335171112:109,877,596G/A—pathogenic
rs20007897912:109,878,572G/A—uncertain significance
rs37208418412:109,878,576G/A—uncertain significance
rs37306908712:109,878,621C/T—uncertain significance
rs77926546212:109,879,493C/T—uncertain significance
rs1106659112:109,880,523G/Adownstream gene variant—
rs11417347912:109,880,977G/T——
rs76452290012:109,881,352G/A—uncertain significance
rs20215146212:109,881,371G/A—uncertain significance
rs75783073012:109,881,434T/C—uncertain significance
rs36900953712:109,882,246G/C—uncertain significance
rs18385740612:109,882,266G/A—benign
rs134656058712:109,882,273G/T—uncertain significance
rs76370335312:109,882,327C/G—uncertain significance
rs14131420612:109,883,338C/T—uncertain significance

Showing 100 of 102 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.