WSCD2
WSC domain containing 2
Summary
Predicted to enable sulfotransferase activity. Predicted to be located in Golgi membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants44 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs4964231 | 12:108,546,543 | G/T | — | — |
| rs181947843 | 12:108,547,387 | G/A | intron variant | — |
| rs199708893 | 12:108,589,662 | G/A | — | uncertain significance |
| rs527323878 | 12:108,589,702 | C/A | — | uncertain significance |
| rs752570341 | 12:108,589,739 | G/A | — | uncertain significance |
| rs778472418 | 12:108,589,784 | G/A | — | uncertain significance |
| rs759121769 | 12:108,589,815 | A/T | — | uncertain significance |
| rs751748620 | 12:108,589,847 | G/A | — | uncertain significance |
| rs368781045 | 12:108,589,856 | T/C | — | uncertain significance |
| rs571473218 | 12:108,589,868 | C/T | — | uncertain significance |
| rs187550758 | 12:108,589,947 | G/C | — | uncertain significance |
| rs201631606 | 12:108,589,971 | G/A | — | uncertain significance |
| rs4964656 | 12:108,594,069 | G/C | intron variant | — |
| rs3794260 | 12:108,598,274 | G/A | intron variant | — |
| rs773674175 | 12:108,600,114 | G/A | — | uncertain significance |
| rs527943874 | 12:108,600,141 | A/T | — | uncertain significance |
| rs1158584686 | 12:108,600,155 | C/T | — | uncertain significance |
| rs7313402 | 12:108,602,970 | C/A | intron variant | — |
| rs771199825 | 12:108,604,028 | G/A | — | uncertain significance |
| rs2137102365 | 12:108,604,034 | C/T | — | uncertain significance |
| rs374953285 | 12:108,604,077 | G/T | — | uncertain significance |
| rs199888315 | 12:108,618,553 | C/G | — | likely benign |
| rs183614363 | 12:108,618,554 | G/A | — | uncertain significance |
| rs201886947 | 12:108,618,567 | T/A | — | uncertain significance |
| rs3764002 | 12:108,618,630 | T/C | — | benign |
| rs371020572 | 12:108,620,770 | T/C | — | uncertain significance |
| rs771571679 | 12:108,620,774 | C/T | — | uncertain significance |
| rs766466339 | 12:108,620,795 | C/A | — | uncertain significance |
| rs371724221 | 12:108,620,831 | C/T | — | uncertain significance |
| rs180963117 | 12:108,620,883 | G/C | — | uncertain significance |
| rs371743603 | 12:108,620,899 | G/A | — | uncertain significance |
| rs770853669 | 12:108,626,552 | C/A | — | uncertain significance |
| rs1426371 | 12:108,629,780 | G/A | regulatory region variant | — |
| rs368092771 | 12:108,634,152 | C/G | — | uncertain significance |
| rs772336574 | 12:108,634,205 | C/A | — | uncertain significance |
| rs749320126 | 12:108,634,268 | G/T | — | uncertain significance |
| rs75980172 | 12:108,636,901 | G/A | intron variant | — |
| rs201772868 | 12:108,641,785 | A/G | — | uncertain significance |
| rs144706841 | 12:108,641,799 | G/A | — | benign |
| rs41314115 | 12:108,641,920 | G/A | — | uncertain significance |
| rs370666947 | 12:108,641,976 | C/A | — | uncertain significance |
| rs374517422 | 12:108,642,080 | G/A | — | uncertain significance |
| rs764803412 | 12:108,642,089 | C/T | — | uncertain significance |
| rs9739493 | 12:108,644,189 | T/C | 3 prime UTR variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.