Gene entry
RTTN
rotatin
- Chromosome
- 18
- Cytoband
- 18q22.2
- Variants (rsID)
- 49
RTTN is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 18 (region 18q22.2). Its official name is “rotatin”. The reference table lists 49 variants (rsID) for this gene.
Clinically classified variants
14 reference-table entries with clinical significance.
- rs117843366Benignsingle nucleotide variant
- rs141156594Benignsingle nucleotide variant
- rs145976466Benignsingle nucleotide variant
- rs17082206Benignsingle nucleotide variant
- rs34353615Benignsingle nucleotide variant
- rs34717557Benignsingle nucleotide variant
- rs35139926Benignsingle nucleotide variant
- rs75225724Benignsingle nucleotide variantMicrocephalic primordial dwarfism due to RTTN deficiency
- rs200600259Conflicting interpretationssingle nucleotide variant
- rs201253231Conflicting interpretationssingle nucleotide variant
- rs35313369Conflicting interpretationssingle nucleotide variant
- rs12956068Likely benignsingle nucleotide variant
- rs201884120Uncertain significancesingle nucleotide variantMICROCEPHALY, SHORT STATURE, AND POLYMICROGYRIA WITH SEIZURES
- rs77798966Uncertain significancesingle nucleotide variant
Other listed variants
- rs1545071
- rs4393674
- rs4891825
- rs10513992
- rs11665578
- rs17082051
- rs17082142
- rs28553277
- rs62089130
- rs74354155
- rs75356692
- rs75621658
- rs76021241
- rs76091143
- rs77360364
- rs77760128
- rs78545564
- rs80021646
- rs80200840
- rs113288937
- rs116851807
- rs116938232
- rs117190313
- rs117538730
- rs117758862
- rs117789537
- rs142016609
- rs142207270
- rs143585515
- rs189284940
- rs191678902
- rs200035293
- rs200376152
- rs201333999
- rs201800329
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.