RGS22
regulator of G protein signaling 22
Summary
Enables G-protein alpha-subunit binding activity. Predicted to be involved in negative regulation of signal transduction. Located in actin cytoskeleton; cytosol; and fibrillar center. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants75 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs139157188 | 8:100,974,669 | A/G | — | benign |
| rs73699897 | 8:100,975,171 | T/C | — | benign |
| rs754175544 | 8:100,975,194 | A/G | — | uncertain significance |
| rs760451465 | 8:100,977,567 | C/T | — | uncertain significance |
| rs187452253 | 8:100,977,655 | C/T | — | uncertain significance |
| rs758064565 | 8:100,990,155 | T/A | — | uncertain significance |
| rs368573670 | 8:100,990,159 | C/T | — | uncertain significance |
| rs949781853 | 8:100,990,179 | T/A | — | uncertain significance |
| rs551799426 | 8:100,994,202 | C/T | — | uncertain significance |
| rs765837823 | 8:100,994,289 | A/G | — | uncertain significance |
| rs376301062 | 8:100,999,715 | G/C | — | uncertain significance |
| rs28765982 | 8:101,007,337 | A/C | intron variant | — |
| rs2199333 | 8:101,011,348 | C/G | — | — |
| rs748996221 | 8:101,011,504 | G/A | — | uncertain significance |
| rs750137458 | 8:101,014,441 | G/C | — | uncertain significance |
| rs765900375 | 8:101,014,552 | T/C | — | uncertain significance |
| rs201197901 | 8:101,014,580 | C/T | — | uncertain significance |
| rs781284660 | 8:101,016,226 | T/C | — | uncertain significance |
| rs199671653 | 8:101,016,292 | G/A | — | uncertain significance |
| rs556859889 | 8:101,016,310 | A/G | — | uncertain significance |
| rs1391759147 | 8:101,018,255 | T/C | — | uncertain significance |
| rs201745883 | 8:101,020,676 | T/C | — | uncertain significance |
| rs187755012 | 8:101,020,754 | A/G | — | uncertain significance |
| rs200812148 | 8:101,020,779 | C/T | — | likely benign |
| rs7006527 | 8:101,024,505 | A/T | — | — |
| rs6989943 | 8:101,028,239 | G/A | intron variant | — |
| rs3133683 | 8:101,033,174 | C/G | — | — |
| rs182407376 | 8:101,037,005 | G/A | upstream gene variant | — |
| rs527775461 | 8:101,038,403 | C/T | — | — |
| rs10283388 | 8:101,044,794 | T/C | intron variant | — |
| rs28884287 | 8:101,047,448 | C/T | intron variant | — |
| rs141050864 | 8:101,049,186 | C/T | intron variant | — |
| rs749509266 | 8:101,051,171 | G/C | — | uncertain significance |
| rs1218332666 | 8:101,051,199 | T/C | — | uncertain significance |
| rs763868756 | 8:101,051,220 | G/A | — | uncertain significance |
| rs188713602 | 8:101,054,074 | T/G | — | uncertain significance |
| rs1233574964 | 8:101,054,134 | T/C | — | likely benign |
| rs749176528 | 8:101,059,709 | T/A | — | uncertain significance |
| rs368946577 | 8:101,059,739 | C/T | — | uncertain significance |
| rs181935065 | 8:101,059,786 | G/T | — | likely benign |
| rs10099237 | 8:101,062,138 | G/C | intron variant | — |
| rs747602476 | 8:101,065,040 | G/C | — | uncertain significance |
| rs779466148 | 8:101,065,050 | G/A | — | uncertain significance |
| rs754676646 | 8:101,065,101 | G/T | — | uncertain significance |
| rs374172601 | 8:101,065,130 | C/T | — | uncertain significance |
| rs137870439 | 8:101,065,134 | G/T | — | uncertain significance |
| rs144398130 | 8:101,065,522 | C/A | — | — |
| rs529196919 | 8:101,066,320 | C/A | — | — |
| rs76022463 | 8:101,071,918 | G/T | intron variant | — |
| rs2488880639 | 8:101,075,722 | G/C | — | uncertain significance |
| rs2488880897 | 8:101,075,743 | A/C | — | uncertain significance |
| rs2488881060 | 8:101,075,755 | T/C | — | uncertain significance |
| rs755990683 | 8:101,075,916 | A/C | — | uncertain significance |
| rs371403021 | 8:101,075,921 | A/G | — | likely benign |
| rs994453098 | 8:101,076,085 | C/T | — | uncertain significance |
| rs757947121 | 8:101,076,148 | T/C | — | uncertain significance |
| rs1714657520 | 8:101,076,184 | T/C | — | uncertain significance |
| rs78300820 | 8:101,076,252 | A/G | — | benign |
| rs775639903 | 8:101,076,270 | C/A | — | uncertain significance |
| rs200474479 | 8:101,078,441 | A/C | — | uncertain significance |
| rs2488903504 | 8:101,078,455 | A/C | — | uncertain significance |
| rs2488904459 | 8:101,078,518 | A/G | — | uncertain significance |
| rs761369913 | 8:101,083,608 | A/T | — | uncertain significance |
| rs2488937766 | 8:101,083,652 | G/A | — | uncertain significance |
| rs140892038 | 8:101,083,683 | C/T | — | uncertain significance |
| rs752894416 | 8:101,083,725 | C/T | — | uncertain significance |
| rs369843131 | 8:101,084,437 | T/C | — | uncertain significance |
| rs867442961 | 8:101,084,439 | C/T | — | uncertain significance |
| rs377393990 | 8:101,092,401 | G/A | — | likely benign |
| rs1024418694 | 8:101,092,468 | C/T | — | uncertain significance |
| rs113394050 | 8:101,096,089 | T/C | regulatory region variant | — |
| rs147879096 | 8:101,105,729 | A/G | — | benign |
| rs190085213 | 8:101,113,835 | G/A | intron variant | — |
| rs1813848408 | 8:101,117,613 | C/T | — | uncertain significance |
| rs899255427 | 8:101,118,128 | C/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.