Gene entry
RP1
RP1 axonemal microtubule associated
- Chromosome
- 8
- Cytoband
- 8q11.23-q12.1
- Variants (rsID)
- 61
RP1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 8 (region 8q11.23-q12.1). Its official name is “RP1 axonemal microtubule associated”. The reference table lists 61 variants (rsID) for this gene.
Clinically classified variants
8 reference-table entries with clinical significance.
- rs113793810Benignsingle nucleotide variantRetinitis pigmentosa
- rs186571865Benignsingle nucleotide variantRetinitis pigmentosa
- rs446227Benignsingle nucleotide variantRetinitis pigmentosa|Autosomal recessive retinitis pigmentosa|Retinitis pigmentosa 1
- rs77775126Benignsingle nucleotide variantRetinitis pigmentosa 1|Retinitis pigmentosa
- rs118031911Conflicting interpretationssingle nucleotide variantRetinitis pigmentosa|Retinitis pigmentosa 1
- rs149282954Conflicting interpretationssingle nucleotide variantRetinitis pigmentosa
- rs189145468Conflicting interpretationssingle nucleotide variantRetinitis pigmentosa
- rs104894082Pathogenicsingle nucleotide variantRetinitis pigmentosa 1|Retinal dystrophy
Other listed variants
- rs454329
- rs768122
- rs1498189
- rs1873963
- rs4355747
- rs4737619
- rs4739035
- rs6473944
- rs6990422
- rs7001303
- rs7009744
- rs7010943
- rs7832057
- rs9298506
- rs9657161
- rs10085958
- rs10102164
- rs10105032
- rs10958432
- rs11781152
- rs13278605
- rs74467533
- rs75613390
- rs75736542
- rs77063236
- rs77598612
- rs77645749
- rs77675038
- rs78140512
- rs80087689
- rs113202934
- rs114511121
- rs116866597
- rs116932954
- rs117070215
- rs117087760
- rs117477226
- rs117850168
- rs117926607
- rs118129580
- rs140033340
- rs141992026
- rs143494598
- rs144115808
- rs146192677
- rs147614445
- rs150906117
- rs151328121
- rs186767020
- rs187676717
- rs190484195
- rs199756880
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.