CHSY3
chondroitin sulfate synthase 3
Summary
CSS3 is a glycosyltransferase that has both glucuronyltransferase and N-acetylgalactosaminyltransferase activities (Yada et al., 2003 [PubMed 12907687]).[supplied by OMIM, Mar 2008]
Known Variants67 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs33918 | 5:129,240,232 | C/T | regulatory region variant | — |
| rs774226347 | 5:129,240,680 | C/T | — | uncertain significance |
| rs1409180227 | 5:129,240,686 | C/A | — | uncertain significance |
| rs566129973 | 5:129,240,719 | C/T | — | likely benign |
| rs746634178 | 5:129,240,727 | C/G | — | uncertain significance |
| rs780522431 | 5:129,240,734 | G/C | — | uncertain significance |
| rs535036047 | 5:129,240,764 | A/G | — | uncertain significance |
| rs2479854399 | 5:129,240,802 | G/A | — | uncertain significance |
| rs1012958799 | 5:129,240,943 | G/A | — | uncertain significance |
| rs1471629987 | 5:129,240,955 | C/T | — | uncertain significance |
| rs925007820 | 5:129,240,959 | G/C | — | uncertain significance |
| rs775342100 | 5:129,240,988 | G/C | — | uncertain significance |
| rs535233532 | 5:129,241,001 | G/A | — | uncertain significance |
| rs768480918 | 5:129,241,033 | G/C | — | uncertain significance |
| rs369526508 | 5:129,241,112 | G/A | — | uncertain significance |
| rs1196814206 | 5:129,241,172 | C/G | — | uncertain significance |
| rs1760246661 | 5:129,241,196 | C/G | — | uncertain significance |
| rs139824617 | 5:129,241,274 | T/C | — | uncertain significance |
| rs2479857275 | 5:129,241,290 | G/T | — | uncertain significance |
| rs146180146 | 5:129,243,821 | A/T | — | uncertain significance |
| rs752938410 | 5:129,243,952 | A/G | — | uncertain significance |
| rs371776468 | 5:129,243,956 | G/T | — | uncertain significance |
| rs201625556 | 5:129,243,967 | A/G | — | uncertain significance |
| rs763048701 | 5:129,244,012 | G/A | — | uncertain significance |
| rs10079258 | 5:129,321,156 | T/A | — | — |
| rs4836487 | 5:129,351,499 | A/G | intron variant | — |
| rs2530251 | 5:129,420,295 | A/G | — | — |
| rs192497898 | 5:129,467,164 | A/T | intron variant | — |
| rs148654806 | 5:129,519,928 | C/A | — | uncertain significance |
| rs765897274 | 5:129,519,956 | A/G | — | uncertain significance |
| rs959475642 | 5:129,519,959 | G/A | — | uncertain significance |
| rs963488186 | 5:129,520,006 | A/G | — | uncertain significance |
| rs2479481993 | 5:129,520,157 | A/C | — | uncertain significance |
| rs201037524 | 5:129,520,221 | A/C | — | uncertain significance |
| rs374972484 | 5:129,520,293 | C/A | — | uncertain significance |
| rs1770354645 | 5:129,520,302 | C/G | — | uncertain significance |
| rs1770355677 | 5:129,520,325 | A/G | — | uncertain significance |
| rs143055952 | 5:129,520,330 | G/A | — | uncertain significance |
| rs757450173 | 5:129,520,342 | A/G | — | uncertain significance |
| rs745713014 | 5:129,520,354 | A/G | — | uncertain significance |
| rs1770360115 | 5:129,520,396 | G/A | — | uncertain significance |
| rs200876793 | 5:129,520,415 | G/T | — | uncertain significance |
| rs779959676 | 5:129,520,459 | C/T | — | uncertain significance |
| rs2479484113 | 5:129,520,559 | C/T | — | uncertain significance |
| rs1294397411 | 5:129,520,572 | T/G | — | uncertain significance |
| rs753729940 | 5:129,520,595 | T/A | — | uncertain significance |
| rs750520567 | 5:129,520,682 | A/C | — | uncertain significance |
| rs373484838 | 5:129,520,708 | G/C | — | uncertain significance |
| rs1452298697 | 5:129,520,714 | C/G | — | uncertain significance |
| rs145272862 | 5:129,520,720 | G/A | — | uncertain significance |
| rs147357375 | 5:129,520,767 | G/T | — | uncertain significance |
| rs369832115 | 5:129,520,768 | T/C | — | uncertain significance |
| rs2479485247 | 5:129,520,825 | G/A | — | uncertain significance |
| rs370684547 | 5:129,520,862 | G/A | — | likely benign |
| rs1335060191 | 5:129,520,900 | A/C | — | uncertain significance |
| rs1257109008 | 5:129,520,925 | G/T | — | uncertain significance |
| rs752010144 | 5:129,521,023 | C/G | — | uncertain significance |
| rs769764138 | 5:129,521,039 | C/A | — | uncertain significance |
| rs1420488939 | 5:129,521,141 | C/T | — | uncertain significance |
| rs746758769 | 5:129,521,212 | G/A | — | uncertain significance |
| rs112623718 | 5:129,521,231 | C/T | — | uncertain significance |
| rs1376865377 | 5:129,521,240 | G/T | — | uncertain significance |
| rs1301107619 | 5:129,521,266 | T/C | — | uncertain significance |
| rs746888153 | 5:129,521,308 | C/G | — | uncertain significance |
| rs143863397 | 5:129,521,401 | A/C | — | uncertain significance |
| rs148231534 | 5:129,521,409 | C/T | — | likely benign |
| rs371008888 | 5:129,521,410 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.