RIPOR3
RIPOR family member 3
Known Variants100 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2515623182 | 20:49,203,855 | A/T | — | uncertain significance |
| rs373302861 | 20:49,203,858 | G/A | — | uncertain significance |
| rs373645112 | 20:49,204,359 | C/T | — | uncertain significance |
| rs200645158 | 20:49,204,372 | G/A | — | uncertain significance |
| rs548944540 | 20:49,204,375 | C/T | — | uncertain significance |
| rs1392337272 | 20:49,204,381 | C/T | — | uncertain significance |
| rs1060402 | 20:49,205,095 | G/A | regulatory region variant | — |
| rs7508819 | 20:49,205,320 | C/A | — | — |
| rs201535929 | 20:49,206,267 | C/T | — | uncertain significance |
| rs371046060 | 20:49,208,889 | G/A | — | uncertain significance |
| rs753109196 | 20:49,208,922 | G/A | — | uncertain significance |
| rs762392679 | 20:49,208,987 | G/A | — | uncertain significance |
| rs202086971 | 20:49,209,017 | C/T | — | uncertain significance |
| rs368643774 | 20:49,209,041 | A/C | — | uncertain significance |
| rs202129855 | 20:49,209,056 | G/A | — | uncertain significance |
| rs200944190 | 20:49,209,602 | C/T | — | uncertain significance |
| rs781035325 | 20:49,209,614 | C/T | — | uncertain significance |
| rs374189330 | 20:49,209,674 | G/T | — | uncertain significance |
| rs766262029 | 20:49,209,686 | G/A | — | uncertain significance |
| rs557718859 | 20:49,209,727 | C/T | — | uncertain significance |
| rs372814425 | 20:49,209,728 | G/A | — | uncertain significance |
| rs201691968 | 20:49,211,161 | G/A | — | uncertain significance |
| rs371910395 | 20:49,211,164 | G/A | — | uncertain significance |
| rs566408535 | 20:49,211,914 | A/G | — | uncertain significance |
| rs773955348 | 20:49,211,956 | A/G | — | uncertain significance |
| rs201715374 | 20:49,211,969 | C/T | — | uncertain significance |
| rs367600299 | 20:49,212,029 | G/A | — | uncertain significance |
| rs184314239 | 20:49,212,036 | C/T | synonymous variant | — |
| rs747405056 | 20:49,212,688 | C/G | — | uncertain significance |
| rs564876086 | 20:49,212,739 | C/T | — | uncertain significance |
| rs189232949 | 20:49,212,762 | G/A | — | uncertain significance |
| rs377276576 | 20:49,212,780 | G/T | — | uncertain significance |
| rs766461315 | 20:49,212,792 | C/T | — | uncertain significance |
| rs749791315 | 20:49,214,121 | G/A | — | uncertain significance |
| rs2515667651 | 20:49,214,125 | C/G | — | uncertain significance |
| rs768411050 | 20:49,214,207 | A/G | — | uncertain significance |
| rs771729586 | 20:49,218,679 | G/A | — | uncertain significance |
| rs370389293 | 20:49,218,725 | C/T | — | uncertain significance |
| rs139663528 | 20:49,218,769 | C/T | — | uncertain significance |
| rs748939000 | 20:49,218,770 | C/T | — | uncertain significance |
| rs759898087 | 20:49,218,774 | C/G | — | uncertain significance |
| rs369361044 | 20:49,218,811 | C/A | — | uncertain significance |
| rs777272607 | 20:49,218,823 | C/A | — | uncertain significance |
| rs748777109 | 20:49,218,824 | T/G | — | uncertain significance |
| rs887137638 | 20:49,218,829 | C/T | — | uncertain significance |
| rs770515279 | 20:49,218,836 | C/A | — | uncertain significance |
| rs547477605 | 20:49,218,885 | G/T | — | uncertain significance |
| rs143391717 | 20:49,218,923 | C/G | — | uncertain significance |
| rs571041619 | 20:49,218,959 | C/T | — | uncertain significance |
| rs2515689704 | 20:49,218,965 | T/C | — | likely benign |
| rs1359395467 | 20:49,219,015 | G/A | — | uncertain significance |
| rs2515690458 | 20:49,219,047 | C/T | — | uncertain significance |
| rs771175438 | 20:49,219,053 | A/G | — | likely benign |
| rs761811071 | 20:49,219,090 | C/T | — | likely benign |
| rs138287130 | 20:49,219,097 | C/T | — | uncertain significance |
| rs376896594 | 20:49,219,142 | C/T | — | uncertain significance |
| rs201353731 | 20:49,221,198 | C/T | — | uncertain significance |
| rs149363568 | 20:49,221,216 | G/A | — | uncertain significance |
| rs200321231 | 20:49,221,270 | G/A | — | uncertain significance |
| rs781525893 | 20:49,221,296 | C/G | — | uncertain significance |
| rs116905185 | 20:49,221,303 | T/C | — | likely benign |
| rs202221804 | 20:49,224,962 | A/C | — | uncertain significance |
| rs1482302878 | 20:49,224,978 | C/T | — | uncertain significance |
| rs780922865 | 20:49,224,981 | C/T | — | uncertain significance |
| rs779903496 | 20:49,224,983 | A/C | — | uncertain significance |
| rs545982151 | 20:49,224,996 | G/A | — | uncertain significance |
| rs772642215 | 20:49,224,998 | G/A | — | uncertain significance |
| rs754931644 | 20:49,225,046 | G/A | — | uncertain significance |
| rs752247003 | 20:49,225,058 | C/T | — | uncertain significance |
| rs146867553 | 20:49,225,158 | C/A | — | uncertain significance |
| rs200366680 | 20:49,225,175 | G/A | — | uncertain significance |
| rs1441323738 | 20:49,225,216 | G/C | — | uncertain significance |
| rs747279590 | 20:49,225,227 | C/T | — | uncertain significance |
| rs567479170 | 20:49,225,257 | G/A | — | uncertain significance |
| rs766766218 | 20:49,225,884 | G/T | — | uncertain significance |
| rs148332840 | 20:49,225,893 | C/T | — | uncertain significance |
| rs150236153 | 20:49,226,115 | C/T | — | likely benign |
| rs1470135745 | 20:49,226,133 | G/T | — | uncertain significance |
| rs763527304 | 20:49,226,171 | G/A | — | uncertain significance |
| rs771513930 | 20:49,226,172 | G/A | — | uncertain significance |
| rs774601813 | 20:49,226,181 | G/A | — | uncertain significance |
| rs761584594 | 20:49,226,192 | C/T | — | likely benign |
| rs765089467 | 20:49,226,193 | G/A | — | uncertain significance |
| rs750130726 | 20:49,226,196 | G/C | — | uncertain significance |
| rs2515725630 | 20:49,226,210 | C/G | — | uncertain significance |
| rs61734272 | 20:49,226,211 | C/T | — | uncertain significance |
| rs6020636 | 20:49,226,496 | A/C | downstream gene variant | — |
| rs767536563 | 20:49,227,726 | G/C | — | uncertain significance |
| rs2515568355 | 20:49,232,561 | T/C | — | uncertain significance |
| rs147229572 | 20:49,232,571 | G/A | — | uncertain significance |
| rs775770067 | 20:49,236,589 | G/A | — | uncertain significance |
| rs2515594363 | 20:49,236,592 | C/A | — | uncertain significance |
| rs145939916 | 20:49,236,604 | G/A | — | uncertain significance |
| rs775867965 | 20:49,236,629 | C/T | — | uncertain significance |
| rs754530233 | 20:49,247,290 | T/C | — | uncertain significance |
| rs200433364 | 20:49,247,309 | C/T | — | uncertain significance |
| rs545666695 | 20:49,247,318 | C/T | — | uncertain significance |
| rs371121479 | 20:49,247,323 | C/T | — | uncertain significance |
| rs141033220 | 20:49,247,330 | C/T | — | uncertain significance |
| rs149834652 | 20:49,247,335 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.