QSER1
glutamine and serine rich 1
Summary
Predicted to be located in chromosome. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants79 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2249555 | 11:32,925,802 | A/G | intron variant | — |
| rs200687979 | 11:32,953,519 | C/A | — | uncertain significance |
| rs766717922 | 11:32,953,584 | T/C | — | likely benign |
| rs2494398527 | 11:32,953,592 | A/G | — | uncertain significance |
| rs541145992 | 11:32,953,803 | A/G | — | likely benign |
| rs769610204 | 11:32,953,886 | C/G | — | uncertain significance |
| rs1852061822 | 11:32,953,898 | G/C | — | uncertain significance |
| rs529763973 | 11:32,953,903 | A/G | — | likely benign |
| rs748950539 | 11:32,953,916 | C/T | — | uncertain significance |
| rs532320073 | 11:32,954,012 | C/T | — | uncertain significance |
| rs1056546715 | 11:32,954,054 | C/T | — | uncertain significance |
| rs761333688 | 11:32,954,125 | C/A | — | uncertain significance |
| rs754336904 | 11:32,954,152 | T/C | — | uncertain significance |
| rs2494402131 | 11:32,954,303 | C/G | — | uncertain significance |
| rs183558161 | 11:32,954,364 | G/A | — | likely benign |
| rs760832988 | 11:32,954,505 | C/G | — | uncertain significance |
| rs375535257 | 11:32,954,614 | T/C | — | uncertain significance |
| rs978359196 | 11:32,954,629 | C/T | — | uncertain significance |
| rs750333325 | 11:32,954,630 | G/A | — | uncertain significance |
| rs779886845 | 11:32,954,677 | A/G | — | uncertain significance |
| rs371820197 | 11:32,954,729 | A/G | — | uncertain significance |
| rs2494405254 | 11:32,954,886 | A/G | — | likely benign |
| rs1852084748 | 11:32,954,941 | A/G | — | uncertain significance |
| rs755326523 | 11:32,954,950 | G/A | — | uncertain significance |
| rs748441560 | 11:32,954,953 | G/A | — | uncertain significance |
| rs760631758 | 11:32,954,989 | T/G | — | uncertain significance |
| rs2494405692 | 11:32,955,001 | G/A | — | uncertain significance |
| rs755499370 | 11:32,955,055 | A/C | — | uncertain significance |
| rs916598784 | 11:32,955,065 | C/T | — | uncertain significance |
| rs376278612 | 11:32,955,076 | T/A | — | uncertain significance |
| rs773036539 | 11:32,955,317 | A/G | — | uncertain significance |
| rs1852093990 | 11:32,955,368 | T/C | — | uncertain significance |
| rs377106160 | 11:32,955,392 | A/C | — | uncertain significance |
| rs375892804 | 11:32,955,490 | T/C | — | uncertain significance |
| rs1320936699 | 11:32,955,546 | A/T | — | uncertain significance |
| rs746528148 | 11:32,955,572 | T/C | — | uncertain significance |
| rs2494408144 | 11:32,955,576 | A/T | — | uncertain significance |
| rs777222714 | 11:32,955,577 | A/G | — | uncertain significance |
| rs2494408174 | 11:32,955,581 | A/G | — | uncertain significance |
| rs376287754 | 11:32,955,653 | A/G | — | uncertain significance |
| rs2494408604 | 11:32,955,679 | C/T | — | uncertain significance |
| rs750245972 | 11:32,955,686 | C/T | — | uncertain significance |
| rs771338526 | 11:32,955,926 | A/G | — | uncertain significance |
| rs753611327 | 11:32,955,973 | G/A | — | uncertain significance |
| rs752356921 | 11:32,955,989 | T/G | — | uncertain significance |
| rs868373139 | 11:32,955,994 | G/C | — | uncertain significance |
| rs200145130 | 11:32,956,006 | A/G | — | uncertain significance |
| rs759281850 | 11:32,956,085 | C/G | — | uncertain significance |
| rs201085763 | 11:32,956,127 | A/G | — | uncertain significance |
| rs2494410924 | 11:32,956,153 | G/A | — | uncertain significance |
| rs375184845 | 11:32,956,259 | G/A | — | uncertain significance |
| rs200456176 | 11:32,956,260 | T/A | — | uncertain significance |
| rs769815493 | 11:32,956,297 | A/G | — | likely benign |
| rs200226940 | 11:32,956,363 | A/C | — | uncertain significance |
| rs777795473 | 11:32,956,417 | G/A | — | likely benign |
| rs746915352 | 11:32,956,461 | G/C | — | uncertain significance |
| rs769490998 | 11:32,956,493 | G/A | — | uncertain significance |
| rs747004821 | 11:32,956,558 | G/A | — | uncertain significance |
| rs776094450 | 11:32,956,669 | G/A | — | uncertain significance |
| rs765364796 | 11:32,956,703 | G/A | — | uncertain significance |
| rs771671291 | 11:32,956,745 | G/A | — | uncertain significance |
| rs776852137 | 11:32,956,760 | C/G | — | uncertain significance |
| rs373045802 | 11:32,956,795 | C/T | — | uncertain significance |
| rs201406150 | 11:32,956,801 | G/C | — | uncertain significance |
| rs762187036 | 11:32,956,897 | C/T | — | likely benign |
| rs970101932 | 11:32,956,927 | G/A | — | likely benign |
| rs199580773 | 11:32,975,439 | A/G | — | uncertain significance |
| rs1852468246 | 11:32,975,564 | A/G | — | uncertain significance |
| rs201036288 | 11:32,975,622 | T/C | — | uncertain significance |
| rs763664409 | 11:32,976,884 | G/A | — | uncertain significance |
| rs758340348 | 11:32,977,654 | T/C | — | uncertain significance |
| rs2494462648 | 11:32,979,425 | G/A | — | uncertain significance |
| rs374350544 | 11:32,979,497 | G/A | — | likely benign |
| rs4755476 | 11:32,980,428 | G/A | — | — |
| rs770104143 | 11:32,990,646 | G/A | — | uncertain significance |
| rs12293579 | 11:32,990,680 | A/G | — | benign |
| rs375889118 | 11:32,990,684 | T/G | — | uncertain significance |
| rs562229910 | 11:32,994,983 | G/A | — | uncertain significance |
| rs199600834 | 11:32,995,070 | C/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.