QRICH1
glutamine rich 1
Summary
Enables DNA binding activity. Involved in intracellular signal transduction; positive regulation of DNA-templated transcription; and positive regulation of apoptotic process. Located in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants113 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs757870894 | 3:49,067,950 | G/A | — | conflicting classifications of pathogenicity |
| rs140691644 | 3:49,067,951 | C/T | — | benign |
| rs745961172 | 3:49,067,952 | G/A | — | uncertain significance |
| rs2106801893 | 3:49,067,959 | T/C | — | uncertain significance |
| rs780388648 | 3:49,067,968 | T/C | — | uncertain significance |
| rs776378682 | 3:49,067,987 | C/G | — | uncertain significance |
| rs2106802170 | 3:49,068,000 | C/T | — | conflicting classifications of pathogenicity |
| rs1229242051 | 3:49,068,002 | G/C | — | uncertain significance |
| rs2093229974 | 3:49,068,009 | C/T | — | likely pathogenic |
| rs146971607 | 3:49,068,050 | G/A | — | likely benign |
| rs1559920341 | 3:49,068,057 | C/T | — | likely pathogenic |
| rs1559920405 | 3:49,068,094 | T/G | — | uncertain significance |
| rs2471646855 | 3:49,069,640 | A/C | — | uncertain significance |
| rs2106810101 | 3:49,069,674 | T/C | — | uncertain significance |
| rs76812435 | 3:49,069,678 | C/T | — | likely benign |
| rs766806091 | 3:49,069,688 | G/C | — | uncertain significance |
| rs2471648702 | 3:49,070,097 | G/A | — | uncertain significance |
| rs148698795 | 3:49,070,104 | C/T | — | likely benign |
| rs1314981903 | 3:49,070,121 | G/A | — | uncertain significance |
| rs2471648893 | 3:49,070,138 | T/C | — | uncertain significance |
| rs1236702036 | 3:49,070,148 | G/A | — | pathogenic |
| rs2106812365 | 3:49,070,208 | T/C | — | pathogenic |
| rs4974081 | 3:49,070,499 | C/A | — | — |
| rs2106813640 | 3:49,070,564 | G/C | — | likely pathogenic |
| rs2471650800 | 3:49,070,620 | C/A | — | pathogenic |
| rs2093252866 | 3:49,070,641 | C/A | — | likely pathogenic |
| rs2106814058 | 3:49,070,663 | T/C | — | pathogenic |
| rs199507730 | 3:49,074,129 | C/A | — | — |
| rs6446218 | 3:49,075,513 | A/G | — | — |
| rs2106854800 | 3:49,081,822 | C/T | — | likely pathogenic |
| rs1183222372 | 3:49,081,883 | G/A | — | uncertain significance |
| rs2106855069 | 3:49,081,889 | A/C | — | likely pathogenic |
| rs1267494571 | 3:49,081,898 | C/T | — | uncertain significance |
| rs2471680338 | 3:49,083,858 | C/T | — | uncertain significance |
| rs2106862882 | 3:49,083,880 | T/C | — | likely pathogenic |
| rs1440438022 | 3:49,083,911 | C/G | — | uncertain significance |
| rs1559930732 | 3:49,083,923 | G/A | — | pathogenic |
| rs2106863254 | 3:49,083,950 | C/T | — | likely pathogenic |
| rs201882007 | 3:49,083,951 | A/G | — | likely benign |
| rs746059690 | 3:49,083,998 | G/A | — | pathogenic |
| rs189806139 | 3:49,084,020 | G/A | — | benign |
| rs2093343142 | 3:49,084,520 | T/C | — | uncertain significance |
| rs770190545 | 3:49,084,539 | T/C | — | likely benign |
| rs2471682518 | 3:49,084,565 | A/C | — | likely pathogenic |
| rs1203493147 | 3:49,084,577 | C/T | — | uncertain significance |
| rs2471682702 | 3:49,084,604 | A/C | — | uncertain significance |
| rs1559931177 | 3:49,084,640 | G/A | — | pathogenic |
| rs1575335524 | 3:49,084,656 | T/C | — | likely benign |
| rs2471682865 | 3:49,084,663 | A/G | — | uncertain significance |
| rs114353727 | 3:49,089,064 | C/G | intron variant | — |
| rs7373790 | 3:49,090,696 | T/C | intron variant | — |
| rs2471706730 | 3:49,094,318 | G/A | — | pathogenic |
| rs1575347805 | 3:49,094,327 | G/C | — | uncertain significance |
| rs2106903188 | 3:49,094,329 | T/C | — | conflicting classifications of pathogenicity |
| rs779853008 | 3:49,094,342 | T/C | — | uncertain significance |
| rs757974895 | 3:49,094,368 | G/A | — | uncertain significance |
| rs2106903534 | 3:49,094,375 | G/A | — | pathogenic |
| rs867624652 | 3:49,094,388 | T/C | — | uncertain significance |
| rs552759046 | 3:49,094,390 | T/C | — | uncertain significance |
| rs2471707098 | 3:49,094,399 | T/A | — | uncertain significance |
| rs759670784 | 3:49,094,406 | C/T | — | likely benign |
| rs1206930424 | 3:49,094,419 | G/A | — | uncertain significance |
| rs2106903855 | 3:49,094,453 | G/C | — | likely pathogenic |
| rs2106904913 | 3:49,094,678 | G/A | — | uncertain significance |
| rs2471708428 | 3:49,094,746 | C/T | — | uncertain significance |
| rs2093408453 | 3:49,094,782 | G/A | — | conflicting classifications of pathogenicity |
| rs2106905360 | 3:49,094,810 | G/A | — | pathogenic |
| rs2093409022 | 3:49,094,863 | G/A | — | uncertain significance |
| rs2106905658 | 3:49,094,877 | C/A | — | likely pathogenic |
| rs1214501563 | 3:49,094,890 | C/T | — | uncertain significance |
| rs150150394 | 3:49,094,904 | T/C | — | likely benign |
| rs2093409295 | 3:49,094,905 | T/G | — | uncertain significance |
| rs897524034 | 3:49,094,932 | C/T | — | uncertain significance |
| rs2471709228 | 3:49,094,936 | C/G | — | uncertain significance |
| rs76308243 | 3:49,094,987 | C/T | — | benign |
| rs1263364974 | 3:49,095,010 | C/T | — | uncertain significance |
| rs2471709690 | 3:49,095,025 | T/C | — | uncertain significance |
| rs778198417 | 3:49,095,035 | C/T | — | uncertain significance |
| rs934007761 | 3:49,095,040 | T/C | — | uncertain significance |
| rs2471709977 | 3:49,095,077 | G/T | — | uncertain significance |
| rs2106906600 | 3:49,095,092 | G/A | — | pathogenic |
| rs770654886 | 3:49,095,114 | G/T | — | uncertain significance |
| rs1351493829 | 3:49,095,157 | G/T | — | uncertain significance |
| rs761326665 | 3:49,095,177 | C/G | — | uncertain significance |
| rs200634836 | 3:49,095,178 | T/G | — | uncertain significance |
| rs2106907115 | 3:49,095,190 | G/T | — | uncertain significance |
| rs374919403 | 3:49,095,206 | C/T | — | likely benign |
| rs2093411936 | 3:49,095,233 | G/A | — | pathogenic |
| rs375758772 | 3:49,095,261 | G/A | — | likely benign |
| rs145975766 | 3:49,095,297 | C/A | — | likely benign |
| rs2471711139 | 3:49,095,307 | T/A | — | uncertain significance |
| rs2093412592 | 3:49,095,308 | G/A | — | pathogenic |
| rs1377134128 | 3:49,095,325 | T/G | — | uncertain significance |
| rs181686792 | 3:49,106,022 | C/T | intron variant | — |
| rs62262510 | 3:49,111,878 | G/A | intron variant | — |
| rs2471766771 | 3:49,114,159 | G/A | — | likely pathogenic |
| rs2471766903 | 3:49,114,192 | G/A | — | pathogenic |
| rs760383510 | 3:49,114,201 | C/T | — | uncertain significance |
| rs2106982905 | 3:49,114,252 | T/C | — | uncertain significance |
| rs867302903 | 3:49,114,261 | T/C | — | uncertain significance |
Showing 100 of 113 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.