GRID1
glutamate ionotropic receptor delta type subunit 1
Summary
This gene encodes a subunit of glutamate receptor channels. These channels mediate most of the fast excitatory synaptic transmission in the central nervous system and play key roles in synaptic plasticity.[provided by RefSeq, Jan 2009]
Known Variants125 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs76636418 | 10:87,359,435 | A/C | 3 prime UTR variant | — |
| rs2492675345 | 10:87,362,076 | C/T | — | uncertain significance |
| rs200155023 | 10:87,362,110 | G/A | — | uncertain significance |
| rs777504269 | 10:87,362,121 | G/A | — | uncertain significance |
| rs149378540 | 10:87,362,205 | G/A | — | uncertain significance |
| rs778828614 | 10:87,362,307 | C/T | — | uncertain significance |
| rs779461467 | 10:87,362,370 | G/A | — | uncertain significance |
| rs536785868 | 10:87,362,424 | C/T | — | uncertain significance |
| rs1842754225 | 10:87,373,168 | T/C | — | uncertain significance |
| rs199648706 | 10:87,373,174 | G/A | — | uncertain significance |
| rs143286261 | 10:87,373,190 | G/A | — | uncertain significance |
| rs2492702754 | 10:87,373,235 | G/C | — | uncertain significance |
| rs2492703236 | 10:87,373,316 | C/T | — | uncertain significance |
| rs2492716618 | 10:87,379,658 | G/A | — | uncertain significance |
| rs759191167 | 10:87,379,714 | G/A | — | uncertain significance |
| rs377494801 | 10:87,379,729 | G/A | — | uncertain significance |
| rs753353279 | 10:87,397,211 | T/C | — | — |
| rs745323059 | 10:87,407,000 | C/A | — | uncertain significance |
| rs779959152 | 10:87,407,006 | C/T | — | uncertain significance |
| rs2492773058 | 10:87,407,032 | T/C | — | uncertain significance |
| rs2492773292 | 10:87,407,096 | C/T | — | uncertain significance |
| rs2492773302 | 10:87,407,102 | C/G | — | uncertain significance |
| rs75499335 | 10:87,412,940 | G/T | upstream gene variant | — |
| rs117613542 | 10:87,425,288 | C/A | — | — |
| rs146127221 | 10:87,465,134 | C/G | — | — |
| rs754921053 | 10:87,482,809 | C/T | — | pathogenic |
| rs376643348 | 10:87,482,846 | C/A | — | uncertain significance |
| rs762615552 | 10:87,482,863 | T/G | — | uncertain significance |
| rs138984541 | 10:87,482,866 | G/T | — | uncertain significance |
| rs201449834 | 10:87,482,884 | C/T | — | uncertain significance |
| rs1427231614 | 10:87,484,118 | C/T | — | uncertain significance |
| rs1301999565 | 10:87,484,148 | T/C | — | uncertain significance |
| rs141961994 | 10:87,484,156 | G/A | — | uncertain significance |
| rs200595427 | 10:87,484,159 | G/T | — | uncertain significance |
| rs768247766 | 10:87,484,166 | C/A | — | uncertain significance |
| rs746452874 | 10:87,484,307 | T/A | — | uncertain significance |
| rs758893534 | 10:87,484,325 | G/A | — | uncertain significance |
| rs754680308 | 10:87,484,328 | T/C | — | uncertain significance |
| rs755662310 | 10:87,484,342 | C/G | — | uncertain significance |
| rs2306265 | 10:87,484,382 | T/C | — | benign |
| rs778875375 | 10:87,487,632 | T/C | — | uncertain significance |
| rs746737416 | 10:87,487,649 | G/T | — | uncertain significance |
| rs533334388 | 10:87,487,650 | T/C | — | uncertain significance |
| rs750951162 | 10:87,487,668 | C/T | — | uncertain significance |
| rs895133091 | 10:87,487,673 | C/G | — | uncertain significance |
| rs1841781018 | 10:87,487,736 | A/G | — | uncertain significance |
| rs1185527979 | 10:87,487,779 | T/G | — | uncertain significance |
| rs147816099 | 10:87,487,797 | C/T | — | uncertain significance |
| rs2492955413 | 10:87,487,806 | C/T | — | uncertain significance |
| rs3812645 | 10:87,489,317 | T/C | — | benign |
| rs1841800463 | 10:87,489,319 | G/C | — | uncertain significance |
| rs772108088 | 10:87,489,320 | G/T | — | uncertain significance |
| rs569475444 | 10:87,534,693 | G/C | — | — |
| rs56272417 | 10:87,600,141 | T/G | intron variant | — |
| rs7076096 | 10:87,608,460 | C/T | intron variant | — |
| rs74814922 | 10:87,609,968 | G/A | intron variant | — |
| rs118168995 | 10:87,614,335 | C/T | — | uncertain significance |
| rs1432517179 | 10:87,614,367 | G/T | — | uncertain significance |
| rs2492281267 | 10:87,615,811 | C/T | — | uncertain significance |
| rs1289900545 | 10:87,615,859 | G/C | — | uncertain significance |
| rs2492281384 | 10:87,615,877 | C/T | — | uncertain significance |
| rs778681237 | 10:87,628,799 | C/T | — | uncertain significance |
| rs2492306441 | 10:87,628,805 | G/A | — | uncertain significance |
| rs748228467 | 10:87,628,819 | C/A | — | uncertain significance |
| rs143353694 | 10:87,628,834 | G/A | — | uncertain significance |
| rs1277371735 | 10:87,628,835 | T/A | — | uncertain significance |
| rs1311464038 | 10:87,628,850 | C/G | — | uncertain significance |
| rs2492306749 | 10:87,628,858 | G/T | — | uncertain significance |
| rs760195348 | 10:87,628,861 | G/A | — | uncertain significance |
| rs757197628 | 10:87,628,882 | G/A | — | uncertain significance |
| rs1970525 | 10:87,634,924 | C/A | — | — |
| rs76765968 | 10:87,694,292 | T/C | intron variant | — |
| rs10788473 | 10:87,740,753 | C/T | intron variant | — |
| rs7910620 | 10:87,846,959 | C/G | intron variant | — |
| rs150809249 | 10:87,847,807 | C/T | intron variant | — |
| rs117759682 | 10:87,860,515 | C/T | regulatory region variant | — |
| rs12573606 | 10:87,882,302 | G/C | — | — |
| rs11201887 | 10:87,884,110 | T/C | intron variant | — |
| rs2492708848 | 10:87,898,596 | C/A | — | uncertain significance |
| rs368448368 | 10:87,898,623 | C/T | — | uncertain significance |
| rs199714522 | 10:87,898,629 | G/A | — | uncertain significance |
| rs758374211 | 10:87,898,640 | C/T | — | uncertain significance |
| rs1349977226 | 10:87,898,706 | T/C | — | uncertain significance |
| rs773280200 | 10:87,898,728 | C/T | — | uncertain significance |
| rs768009874 | 10:87,898,742 | C/T | — | uncertain significance |
| rs147826442 | 10:87,898,779 | T/C | — | uncertain significance |
| rs7915663 | 10:87,914,036 | T/A | intron variant | — |
| rs7912161 | 10:87,923,404 | G/A | regulatory region variant | — |
| rs12257526 | 10:87,928,843 | T/C | intron variant | — |
| rs12262754 | 10:87,929,082 | G/A | intron variant | — |
| rs184274255 | 10:87,941,024 | G/T | — | — |
| rs11201929 | 10:87,944,571 | G/A | intron variant | — |
| rs749990712 | 10:87,966,127 | C/T | — | uncertain significance |
| rs779659096 | 10:87,966,133 | C/T | — | uncertain significance |
| rs956188880 | 10:87,966,142 | T/C | — | uncertain significance |
| rs202162769 | 10:87,966,145 | C/T | — | uncertain significance |
| rs771100097 | 10:87,966,159 | C/T | — | uncertain significance |
| rs1282622742 | 10:87,966,160 | G/A | — | uncertain significance |
| rs192984874 | 10:87,966,192 | T/C | — | uncertain significance |
| rs201182031 | 10:87,966,199 | G/A | — | benign |
Showing 100 of 125 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.