Gene entry
JMJD1C
jumonji domain containing 1C
- Chromosome
- 10
- Cytoband
- 10q21.3
- Variants (rsID)
- 62
JMJD1C is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 10 (region 10q21.3). Its official name is “jumonji domain containing 1C”. The reference table lists 62 variants (rsID) for this gene.
Clinically classified variants
6 reference-table entries with clinical significance.
- rs117647164Benignsingle nucleotide variantEarly myoclonic encephalopathy
- rs149833441Benignsingle nucleotide variantEarly myoclonic encephalopathy
- rs41274064Benignsingle nucleotide variantEarly myoclonic encephalopathy
- rs41274068Benignsingle nucleotide variantEarly myoclonic encephalopathy
- rs41274072Benignsingle nucleotide variantEarly myoclonic encephalopathy
- rs71508957Likely benignsingle nucleotide variantEarly myoclonic encephalopathy
Other listed variants
- rs2393967
- rs2893923
- rs4291564
- rs6479891
- rs7075195
- rs7896518
- rs7896783
- rs7900050
- rs7906819
- rs7910662
- rs7910927
- rs7923609
- rs10437345
- rs10761779
- rs12250472
- rs12355784
- rs12773283
- rs12773976
- rs16918507
- rs17741598
- rs34736861
- rs35506702
- rs35632171
- rs58005737
- rs61853632
- rs72835365
- rs72835378
- rs72837027
- rs72837044
- rs75160815
- rs75795133
- rs76183377
- rs76519798
- rs76589845
- rs76637437
- rs77915324
- rs78023800
- rs78592316
- rs78842693
- rs79038193
- rs79549948
- rs79766796
- rs80151542
- rs113112594
- rs113262551
- rs116999194
- rs117251861
- rs117286393
- rs117466130
- rs117589535
- rs117637094
- rs117789984
- rs118079335
- rs143262502
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.