Gene entry
DCDC2
doublecortin domain containing 2
- Chromosome
- 6
- Cytoband
- 6p22.3
- Variants (rsID)
- 42
DCDC2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 6 (region 6p22.3). Its official name is “doublecortin domain containing 2”. The reference table lists 42 variants (rsID) for this gene.
Clinically classified variants
5 reference-table entries with clinical significance.
- rs2274305Benignsingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 66|Isolated neonatal sclerosing cholangitis|Isolated neonatal sclerosing cholangitis|Nephronophthisis 19|Autosomal recessive nonsyndromic hearing loss 66
- rs141060456Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 66|Isolated neonatal sclerosing cholangitis
- rs144695853Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 66|Isolated neonatal sclerosing cholangitis
- rs146787541Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 66|Isolated neonatal sclerosing cholangitis
- rs200595563Uncertain significancesingle nucleotide variantIsolated neonatal sclerosing cholangitis|Autosomal recessive nonsyndromic hearing loss 66
Other listed variants
- rs793674
- rs811103
- rs1277351
- rs1340699
- rs1419228
- rs1620407
- rs2791972
- rs2799373
- rs3789219
- rs6456594
- rs7739231
- rs9295616
- rs9393547
- rs9460974
- rs10498720
- rs11962116
- rs12192506
- rs35796857
- rs41304913
- rs62400407
- rs72833035
- rs73394078
- rs74945887
- rs76357407
- rs76864542
- rs78438927
- rs79067286
- rs79581445
- rs113404187
- rs114676109
- rs115151497
- rs115381407
- rs115738635
- rs192323413
- rs201158565
- rs369366892
- rs775169863
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.