Gene entry
STIL
STIL centriolar assembly protein
- Chromosome
- 1
- Cytoband
- 1p33
- Variants (rsID)
- 18
STIL is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1p33). Its official name is “STIL centriolar assembly protein”. The reference table lists 18 variants (rsID) for this gene.
Clinically classified variants
10 reference-table entries with clinical significance.
- rs140975915Benignsingle nucleotide variantMicrocephaly 7, primary, autosomal recessive
- rs142315727Benignsingle nucleotide variantMicrocephaly 7, primary, autosomal recessive
- rs550062989Benignsingle nucleotide variantMicrocephaly 7, primary, autosomal recessive
- rs6697248Benignsingle nucleotide variant
- rs139912214Conflicting interpretationssingle nucleotide variantInborn genetic diseases|Abnormality of brain morphology|Microcephaly 7, primary, autosomal recessive
- rs148193936Conflicting interpretationssingle nucleotide variantMicrocephaly 7, primary, autosomal recessive
- rs149296029Conflicting interpretationssingle nucleotide variantMicrocephaly 7, primary, autosomal recessive
- rs188900275Conflicting interpretationssingle nucleotide variant
- rs368201717Conflicting interpretationssingle nucleotide variant
- rs202194355Uncertain significancesingle nucleotide variantInborn genetic diseases|Microcephaly 7, primary, autosomal recessive
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.