Gene entry
LYST
lysosomal trafficking regulator
- Chromosome
- 1
- Cytoband
- 1q42.3
- Variants (rsID)
- 55
LYST is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1q42.3). Its official name is “lysosomal trafficking regulator”. The reference table lists 55 variants (rsID) for this gene.
Clinically classified variants
23 reference-table entries with clinical significance.
- rs111764031Benignsingle nucleotide variantChédiak-Higashi syndrome|Autoinflammatory syndrome
- rs112601869Benignsingle nucleotide variantChédiak-Higashi syndrome|Autoinflammatory syndrome
- rs17615059Benignsingle nucleotide variant
- rs34642241Benignsingle nucleotide variantChédiak-Higashi syndrome|Autoinflammatory syndrome
- rs77091385Benignsingle nucleotide variantChédiak-Higashi syndrome|Autoinflammatory syndrome
- rs140434436Conflicting interpretationssingle nucleotide variantChédiak-Higashi syndrome|Autoinflammatory syndrome
- rs141317482Conflicting interpretationssingle nucleotide variantChédiak-Higashi syndrome|Autoinflammatory syndrome
- rs147756847Conflicting interpretationssingle nucleotide variantChédiak-Higashi syndrome|Autoinflammatory syndrome
- rs150306354Conflicting interpretationssingle nucleotide variantChédiak-Higashi syndrome|Autoinflammatory syndrome
- rs33998267Conflicting interpretationssingle nucleotide variantChédiak-Higashi syndrome|Autoinflammatory syndrome
- rs372892911Conflicting interpretationssingle nucleotide variantChédiak-Higashi syndrome
- rs72761794Conflicting interpretationssingle nucleotide variantChédiak-Higashi syndrome|Autoinflammatory syndrome
- rs28942077Pathogenicsingle nucleotide variantChediak-Higashi syndrome, adult type|Chédiak-Higashi syndrome
- rs80338642PathogenicDuplicationChediak-Higashi syndrome, childhood type|Chédiak-Higashi syndrome
- rs80338643Pathogenicsingle nucleotide variantChediak-Higashi syndrome, childhood type|Chédiak-Higashi syndrome
- rs80338644PathogenicDeletionChediak-Higashi syndrome, childhood type|Chédiak-Higashi syndrome
- rs80338651Pathogenicsingle nucleotide variantChediak-Higashi syndrome, childhood type|Chédiak-Higashi syndrome
- rs80338652Pathogenicsingle nucleotide variantChediak-Higashi syndrome, adult type|Chédiak-Higashi syndrome
- rs80338657Pathogenicsingle nucleotide variantChediak-Higashi syndrome, adult type|Chédiak-Higashi syndrome
- rs148299757Uncertain significancesingle nucleotide variantChédiak-Higashi syndrome
- rs148409403Uncertain significancesingle nucleotide variantChédiak-Higashi syndrome|Autoinflammatory syndrome
- rs199576020Uncertain significancesingle nucleotide variantChédiak-Higashi syndrome
- rs200231136Uncertain significancesingle nucleotide variantChédiak-Higashi syndrome
Other listed variants
- rs2208384
- rs7513729
- rs7535375
- rs7545788
- rs10802994
- rs10926565
- rs11810173
- rs34341762
- rs35402102
- rs35753830
- rs72761800
- rs75287707
- rs78611805
- rs79679095
- rs112938240
- rs114165158
- rs114177384
- rs115019462
- rs115174118
- rs141509909
- rs144275846
- rs147963856
- rs187257944
- rs188870379
- rs190257717
- rs190975027
- rs200044710
- rs200353560
- rs200437063
- rs200753782
- rs201106245
- rs201502579
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.