Gene entry
GRIA3
glutamate ionotropic receptor AMPA type subunit 3
- Chromosome
- X
- Cytoband
- Xq25
- Variants (rsID)
- 143
GRIA3 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome X (region Xq25). Its official name is “glutamate ionotropic receptor AMPA type subunit 3”. The reference table lists 143 variants (rsID) for this gene.
Clinically classified variants
5 reference-table entries with clinical significance.
- rs138817389Benignsingle nucleotide variantHistory of neurodevelopmental disorder|Syndromic X-linked intellectual disability 94
- rs502434Benignsingle nucleotide variantHistory of neurodevelopmental disorder|Syndromic X-linked intellectual disability 94
- rs139990565Likely pathogenicsingle nucleotide variant
- rs137852351Pathogenicsingle nucleotide variantSyndromic X-linked intellectual disability 94
- rs137852352Pathogenicsingle nucleotide variantSyndromic X-linked intellectual disability 94
Other listed variants
- rs484570
- rs503118
- rs514476
- rs524654
- rs526716
- rs531515
- rs545958
- rs549895
- rs550640
- rs551166
- rs561101
- rs592807
- rs602086
- rs608950
- rs612595
- rs616364
- rs625074
- rs637574
- rs651595
- rs652582
- rs664400
- rs674073
- rs678657
- rs682478
- rs687577
- rs695214
- rs983007
- rs989639
- rs1034426
- rs1557545
- rs1800654
- rs2040404
- rs2157271
- rs2157272
- rs2157292
- rs2157293
- rs2187797
- rs2227098
- rs2269550
- rs2269551
- rs2354037
- rs2511034
- rs3761554
- rs3761555
- rs3827431
- rs3848874
- rs3904733
- rs4825476
- rs4825836
- rs4825838
- rs4825839
- rs4825841
- rs4825847
- rs4825856
- rs4825857
- rs5909978
- rs5909980
- rs5909981
- rs5910002
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.
