Gene entry
MED13L
mediator complex subunit 13L
- Chromosome
- 12
- Cytoband
- 12q24.21
- Variants (rsID)
- 38
MED13L is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 12 (region 12q24.21). Its official name is “mediator complex subunit 13L”. The reference table lists 38 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs869025287PathogenicDeletionCardiac anomalies - developmental delay - facial dysmorphism syndrome|Intellectual disability
Other listed variants
- rs1992069
- rs7314113
- rs10507268
- rs11067898
- rs11067928
- rs11609062
- rs11611238
- rs12312570
- rs12578382
- rs16946512
- rs16946520
- rs17580661
- rs35143779
- rs56159711
- rs73200221
- rs75305186
- rs76712647
- rs77421137
- rs77973800
- rs80064874
- rs80342485
- rs112608219
- rs116909459
- rs116943307
- rs117049763
- rs117454764
- rs117846871
- rs118154624
- rs138246667
- rs141337373
- rs141353737
- rs144203443
- rs146508741
- rs149651647
- rs202075689
- rs867194937
- rs868717689
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.