Gene entry
GRIP1
glutamate receptor interacting protein 1
- Chromosome
- 12
- Cytoband
- 12q14.3
- Variants (rsID)
- 158
GRIP1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 12 (region 12q14.3). Its official name is “glutamate receptor interacting protein 1”. The reference table lists 158 variants (rsID) for this gene.
Clinically classified variants
4 reference-table entries with clinical significance.
- rs1168308Benignsingle nucleotide variantFraser syndrome 3
- rs145115262Benignsingle nucleotide variantFraser syndrome 3|Intellectual disability
- rs150958775Benignsingle nucleotide variantFraser syndrome 3
- rs17102531Benignsingle nucleotide variantFraser syndrome 3
Other listed variants
- rs748528
- rs748529
- rs774378
- rs774381
- rs774392
- rs774398
- rs983665
- rs1008948
- rs1021870
- rs1252262
- rs1252279
- rs1262101
- rs1394266
- rs1472216
- rs1480014
- rs1480020
- rs1480022
- rs1566827
- rs1604842
- rs1871549
- rs1918136
- rs1921012
- rs1982664
- rs2062858
- rs2134833
- rs2904531
- rs3751276
- rs3891950
- rs4283063
- rs4506729
- rs4526844
- rs4540902
- rs4913307
- rs4913353
- rs4913512
- rs4913515
- rs6581710
- rs6581712
- rs7132504
- rs7136159
- rs7136625
- rs7136670
- rs7297817
- rs7300761
- rs7301580
- rs7309118
- rs7310363
- rs7310441
- rs7310442
- rs7342347
- rs7488420
- rs7955073
- rs7961471
- rs7963639
- rs7966884
- rs7975411
- rs10128955
- rs10219488
- rs10506489
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.