Gene entry
DYM
dymeclin
- Chromosome
- 18
- Cytoband
- 18q21.1
- Variants (rsID)
- 58
DYM is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 18 (region 18q21.1). Its official name is “dymeclin”. The reference table lists 58 variants (rsID) for this gene.
Clinically classified variants
6 reference-table entries with clinical significance.
- rs75854087Benignsingle nucleotide variant
- rs138427861Conflicting interpretationssingle nucleotide variantSmith-McCort dysplasia|Dyggve-Melchior-Clausen syndrome
- rs145279594Conflicting interpretationssingle nucleotide variantDyggve-Melchior-Clausen syndrome|Smith-McCort dysplasia
- rs148059981Likely pathogenicsingle nucleotide variant
- rs120074163Pathogenicsingle nucleotide variantDyggve-Melchior-Clausen syndrome
- rs120074164Uncertain significancesingle nucleotide variantSmith-McCort dysplasia 1
Other listed variants
- rs515157
- rs572642
- rs576057
- rs833520
- rs1052695
- rs1787200
- rs2009507
- rs2053515
- rs7229507
- rs7232138
- rs8086876
- rs8089472
- rs9304371
- rs9964222
- rs9967417
- rs11082727
- rs11874863
- rs12456845
- rs12458127
- rs12607069
- rs28470838
- rs35392618
- rs72921661
- rs74806417
- rs75001488
- rs75531197
- rs75694940
- rs76856822
- rs77451458
- rs77485101
- rs78252660
- rs78965095
- rs79973129
- rs111329920
- rs112367671
- rs116866042
- rs117046026
- rs117135818
- rs117248232
- rs117374190
- rs117436411
- rs117843038
- rs118031367
- rs118057683
- rs118088489
- rs140584466
- rs186680474
- rs190980988
- rs200518242
- rs202085847
- rs373012712
- rs577321919
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.