Gene entry
CNGB1
cyclic nucleotide gated channel subunit beta 1
- Chromosome
- 16
- Cytoband
- 16q21
- Variants (rsID)
- 70
CNGB1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 16 (region 16q21). Its official name is “cyclic nucleotide gated channel subunit beta 1”. The reference table lists 70 variants (rsID) for this gene.
Clinically classified variants
21 reference-table entries with clinical significance.
- rs112002818Benignsingle nucleotide variantRetinitis pigmentosa
- rs11867123Benignsingle nucleotide variantRetinitis pigmentosa
- rs12927214Benignsingle nucleotide variantRetinitis pigmentosa
- rs13336595Benignsingle nucleotide variantRetinitis pigmentosa|Retinitis pigmentosa 45
- rs2161703Benignsingle nucleotide variantRetinitis pigmentosa
- rs61745888Benignsingle nucleotide variantRetinitis pigmentosa
- rs61997250Benignsingle nucleotide variantRetinitis pigmentosa
- rs76788887Benignsingle nucleotide variantRetinitis pigmentosa
- rs79889567Benignsingle nucleotide variantRetinitis pigmentosa 45
- rs146170855Conflicting interpretationssingle nucleotide variantRetinitis pigmentosa
- rs147593839Conflicting interpretationssingle nucleotide variantRetinal dystrophy|Retinitis pigmentosa
- rs148999583Conflicting interpretationssingle nucleotide variantRetinitis pigmentosa
- rs199591689Conflicting interpretationssingle nucleotide variantRetinitis pigmentosa|Retinitis pigmentosa 45
- rs200242407Conflicting interpretationssingle nucleotide variantRetinitis pigmentosa
- rs201162411Conflicting interpretationssingle nucleotide variantRetinitis pigmentosa|Retinal dystrophy|Autosomal recessive retinitis pigmentosa|Retinitis pigmentosa 45
- rs201553871Conflicting interpretationssingle nucleotide variantRetinitis pigmentosa 45|Retinitis pigmentosa 49|Retinitis pigmentosa
- rs539304668Conflicting interpretationssingle nucleotide variantRetinitis pigmentosa
- rs78292723Conflicting interpretationssingle nucleotide variantRetinitis pigmentosa
- rs146762538Likely benignsingle nucleotide variantRetinal dystrophy
- rs372504780Pathogenicsingle nucleotide variantRetinitis pigmentosa|Retinal dystrophy
- rs116564376Uncertain significancesingle nucleotide variantRetinitis pigmentosa
Other listed variants
- rs152142
- rs247037
- rs437947
- rs691483
- rs691656
- rs1108645
- rs2161702
- rs3784899
- rs3815950
- rs3848262
- rs3991716
- rs4555144
- rs7184838
- rs7186432
- rs7193726
- rs7206208
- rs8046202
- rs8052097
- rs9922949
- rs11648175
- rs16959471
- rs16959476
- rs16959477
- rs16959513
- rs17240973
- rs35257432
- rs55835827
- rs56097461
- rs58979009
- rs67716117
- rs67957317
- rs72782251
- rs72782267
- rs74019712
- rs75969548
- rs76912005
- rs77014482
- rs78115609
- rs78779042
- rs78944872
- rs79581943
- rs80124781
- rs80255011
- rs113414137
- rs116911900
- rs117318343
- rs117533055
- rs137971619
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.