Gene entry
HMCN1
hemicentin 1
- Chromosome
- 1
- Cytoband
- 1q25.3-q31.1
- Variants (rsID)
- 114
HMCN1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1q25.3-q31.1). Its official name is “hemicentin 1”. The reference table lists 114 variants (rsID) for this gene.
Clinically classified variants
21 reference-table entries with clinical significance.
- rs1056456Benignsingle nucleotide variantAge related macular degeneration 1
- rs10798035Benignsingle nucleotide variantAge related macular degeneration 1
- rs114135070Benignsingle nucleotide variantAge related macular degeneration 1
- rs115169621Benignsingle nucleotide variantAge related macular degeneration 1
- rs116300191Benignsingle nucleotide variantAge related macular degeneration 1
- rs12129650Benignsingle nucleotide variantAge related macular degeneration 1
- rs12239296Benignsingle nucleotide variantAge related macular degeneration 1
- rs139870667Benignsingle nucleotide variantAge related macular degeneration 1
- rs147296385Benignsingle nucleotide variantAge related macular degeneration 1
- rs147851396Benignsingle nucleotide variantAge related macular degeneration 1
- rs41317471Benignsingle nucleotide variantAge related macular degeneration 1
- rs41317489Benignsingle nucleotide variantAge related macular degeneration 1
- rs41317497Benignsingle nucleotide variantAge related macular degeneration 1
- rs6693069Benignsingle nucleotide variantAge related macular degeneration 1
- rs7539719Benignsingle nucleotide variantAge related macular degeneration 1
- rs79183244Benignsingle nucleotide variantAge related macular degeneration 1
- rs76432158Likely benignsingle nucleotide variantAge related macular degeneration 1
- rs145398864Uncertain significancesingle nucleotide variantAge related macular degeneration 1
- rs146671871Uncertain significancesingle nucleotide variantAge related macular degeneration 1
- rs182468717Uncertain significancesingle nucleotide variantAge related macular degeneration 1
- rs369620574Uncertain significancesingle nucleotide variantAge related macular degeneration 1
Other listed variants
- rs586727
- rs743135
- rs1321676
- rs1322376
- rs1407425
- rs1407428
- rs1407434
- rs1471728
- rs1555494
- rs2208692
- rs4141459
- rs4651287
- rs4651295
- rs6677289
- rs6696804
- rs6698721
- rs7546152
- rs7556537
- rs9425349
- rs10489717
- rs10489751
- rs10911836
- rs11586771
- rs12024953
- rs12070701
- rs12078444
- rs12080760
- rs12118857
- rs12144532
- rs16825020
- rs17448230
- rs41317483
- rs41317499
- rs41317501
- rs41317505
- rs41357745
- rs61002359
- rs61829889
- rs61829915
- rs61829929
- rs72733226
- rs74136012
- rs74607760
- rs76014482
- rs76954684
- rs77294353
- rs77460954
- rs77516215
- rs78621181
- rs78806371
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.