Gene entry
RS1
retinoschisin 1
- Chromosome
- X
- Cytoband
- Xp22.13
- Variants (rsID)
- 65
RS1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome X (region Xp22.13). Its official name is “retinoschisin 1”. The reference table lists 65 variants (rsID) for this gene.
Clinically classified variants
51 reference-table entries with clinical significance.
- rs1800002Conflicting interpretationssingle nucleotide variantRetinal dystrophy
- rs61750458Conflicting interpretationsDeletionRetinal dystrophy
- rs61752060Likely pathogenicsingle nucleotide variantJuvenile retinoschisis
- rs61753164Likely pathogenicsingle nucleotide variantRetinal dystrophy
- rs104894929Pathogenicsingle nucleotide variantJuvenile retinoschisis
- rs104894930Pathogenicsingle nucleotide variantJuvenile retinoschisis|Retinal dystrophy|Retinoschisis
- rs104894933Pathogenicsingle nucleotide variantJuvenile retinoschisis
- rs104894934Pathogenicsingle nucleotide variantJuvenile retinoschisis
- rs1801161Pathogenicsingle nucleotide variant
- rs281865348Pathogenicsingle nucleotide variantJuvenile retinoschisis|Retinal dystrophy
- rs281865357Pathogenicsingle nucleotide variantRetinal dystrophy|Juvenile retinoschisis
- rs281865358Pathogenicsingle nucleotide variant
- rs281865362Pathogenicsingle nucleotide variant
- rs281865365Pathogenicsingle nucleotide variantJuvenile retinoschisis
- rs61752062Pathogenicsingle nucleotide variant
- rs61752063Pathogenicsingle nucleotide variantJuvenile retinoschisis|Retinal dystrophy
- rs61752064Pathogenicsingle nucleotide variant
- rs61752067Pathogenicsingle nucleotide variantJuvenile retinoschisis|Retinal dystrophy
- rs61752068Pathogenicsingle nucleotide variantJuvenile retinoschisis|Retinal dystrophy
- rs61752071PathogenicDuplicationRetinal dystrophy
- rs61752145Pathogenicsingle nucleotide variantRetinal dystrophy
- rs61752148PathogenicMicrosatellite
- rs61752153Pathogenicsingle nucleotide variant
- rs61752156Pathogenicsingle nucleotide variantRetinoschisis
- rs61752157Pathogenicsingle nucleotide variant
- rs61752158Pathogenicsingle nucleotide variant
- rs61752159Pathogenicsingle nucleotide variantJuvenile retinoschisis
- rs61753174Pathogenicsingle nucleotide variant
- rs61752069Uncertain significancesingle nucleotide variant
- rs1800001Not classifiedsingle nucleotide variant
- rs61750457Not classifiedsingle nucleotide variant
- rs61750459Not classifiedsingle nucleotide variant
- rs61752061Not classifiedsingle nucleotide variant
- rs61752065Not classifiedsingle nucleotide variant
- rs61752066Not classifiedsingle nucleotide variant
- rs61752070Not classifiedsingle nucleotide variant
- rs61752072Not classifiedsingle nucleotide variant
- rs61752146Not classifiedInsertion
- rs61752147Not classifiedsingle nucleotide variant
- rs61752149Not classifiedsingle nucleotide variant
- rs61752151Not classifiedsingle nucleotide variant
- rs61752152Not classifiedsingle nucleotide variant
- rs61752154Not classifiedsingle nucleotide variant
- rs61753162Not classifiedsingle nucleotide variant
- rs61753165Not classifiedsingle nucleotide variant
- rs61753166Not classifiedsingle nucleotide variant
- rs61753167Not classifiedsingle nucleotide variant
- rs61753168Not classifiedsingle nucleotide variant
- rs61753169Not classifiedsingle nucleotide variant
- rs61753170Not classifiedsingle nucleotide variant
- rs62641252Not classifiedsingle nucleotide variant
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.