Gene entry
MID1
midline 1
- Chromosome
- X
- Cytoband
- Xp22.2
- Variants (rsID)
- 46
MID1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome X (region Xp22.2). Its official name is “midline 1”. The reference table lists 46 variants (rsID) for this gene.
Clinically classified variants
4 reference-table entries with clinical significance.
- rs138629923Conflicting interpretationssingle nucleotide variant
- rs147106995Conflicting interpretationssingle nucleotide variantX-linked Opitz G/BBB syndrome|History of neurodevelopmental disorder
- rs104894866Pathogenicsingle nucleotide variantX-linked Opitz G/BBB syndrome
- rs398123341Uncertain significancesingle nucleotide variant
Other listed variants
- rs685615
- rs741499
- rs869917
- rs960419
- rs974581
- rs1989812
- rs2188374
- rs2525070
- rs5933848
- rs5934908
- rs5978406
- rs5978414
- rs5979317
- rs6530400
- rs6530403
- rs6530404
- rs7051591
- rs7051690
- rs7055659
- rs7057047
- rs7059850
- rs7063354
- rs7065297
- rs7876447
- rs7878745
- rs7886985
- rs7888885
- rs7891302
- rs7892146
- rs7892539
- rs10521613
- rs12007673
- rs12008851
- rs12849558
- rs12852005
- rs12855797
- rs61382997
- rs62589986
- rs75465623
- rs139026561
- rs146802912
- rs201454444
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.