GABRR1
gamma-aminobutyric acid type A receptor subunit rho1
Summary
GABA is the major inhibitory neurotransmitter in the mammalian brain where it acts at GABA receptors, which are ligand-gated chloride channels. GABRR1 is a member of the rho subunit family. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2012]
Known Variants31 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs773678062 | 6:89,888,544 | A/G | — | uncertain significance |
| rs772321848 | 6:89,888,656 | C/T | — | uncertain significance |
| rs1196309553 | 6:89,888,662 | T/A | — | uncertain significance |
| rs1302327803 | 6:89,888,727 | T/C | — | uncertain significance |
| rs202214989 | 6:89,888,745 | G/A | — | likely benign |
| rs1236615217 | 6:89,890,048 | G/A | — | uncertain significance |
| rs549471218 | 6:89,890,064 | C/T | — | uncertain significance |
| rs763072691 | 6:89,890,094 | C/T | — | uncertain significance |
| rs533367206 | 6:89,890,105 | C/T | — | uncertain significance |
| rs192148367 | 6:89,890,145 | C/T | — | uncertain significance |
| rs376401079 | 6:89,890,148 | G/A | — | uncertain significance |
| rs567561851 | 6:89,890,171 | G/A | — | uncertain significance |
| rs767876225 | 6:89,890,177 | A/G | — | uncertain significance |
| rs372557173 | 6:89,891,654 | G/A | — | uncertain significance |
| rs773405441 | 6:89,891,741 | G/A | — | uncertain significance |
| rs1321201510 | 6:89,891,761 | A/G | — | uncertain significance |
| rs370866905 | 6:89,895,100 | C/T | — | uncertain significance |
| rs200602822 | 6:89,895,101 | G/A | — | uncertain significance |
| rs1771872590 | 6:89,895,128 | C/A | — | uncertain significance |
| rs767116686 | 6:89,899,928 | C/T | — | uncertain significance |
| rs973456463 | 6:89,899,950 | T/C | — | uncertain significance |
| rs34218666 | 6:89,907,786 | G/A | — | benign |
| rs201812835 | 6:89,907,817 | C/T | — | uncertain significance |
| rs2533610852 | 6:89,907,824 | A/G | — | uncertain significance |
| rs150775662 | 6:89,907,860 | T/G | — | uncertain significance |
| rs899533371 | 6:89,910,904 | T/C | — | uncertain significance |
| rs1178171800 | 6:89,910,910 | T/G | — | uncertain significance |
| rs750103108 | 6:89,913,162 | C/A | — | uncertain significance |
| rs13215566 | 6:89,918,638 | C/G | intron variant | — |
| rs1186902 | 6:89,926,962 | T/C | missense variant | — |
| rs12200969 | 6:89,926,966 | T/C | missense variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.