SLC7A6OS
solute carrier family 7 member 6 opposite strand
Summary
Predicted to be involved in developmental process. Predicted to act upstream of or within hematopoietic progenitor cell differentiation. Predicted to be located in cytoplasm and nucleus. Implicated in progressive myoclonus epilepsy. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants31 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1178336010 | 16:68,335,189 | C/A | — | uncertain significance |
| rs145382889 | 16:68,336,308 | T/C | — | uncertain significance |
| rs764496408 | 16:68,336,324 | G/C | — | uncertain significance |
| rs2543420203 | 16:68,336,340 | T/C | — | uncertain significance |
| rs2151239071 | 16:68,336,374 | A/G | — | uncertain significance |
| rs6499167 | 16:68,337,798 | T/A | downstream gene variant | — |
| rs202170729 | 16:68,337,937 | A/G | — | uncertain significance |
| rs143239221 | 16:68,337,938 | T/C | — | likely benign |
| rs771210829 | 16:68,337,953 | C/A | — | uncertain significance |
| rs138428124 | 16:68,337,958 | C/T | — | likely benign |
| rs188304848 | 16:68,337,959 | G/A | — | likely benign |
| rs139184366 | 16:68,337,993 | G/A | — | likely benign |
| rs747649057 | 16:68,338,017 | A/G | — | uncertain significance |
| rs56372488 | 16:68,339,734 | C/A | — | — |
| rs889184698 | 16:68,344,242 | C/A | — | uncertain significance |
| rs201365695 | 16:68,344,291 | C/G | — | uncertain significance |
| rs769523136 | 16:68,344,302 | A/T | — | uncertain significance |
| rs142496712 | 16:68,344,329 | T/C | — | likely benign |
| rs2543450224 | 16:68,344,351 | C/T | — | uncertain significance |
| rs535274480 | 16:68,344,357 | C/A | — | uncertain significance |
| rs1394037811 | 16:68,344,393 | G/A | — | uncertain significance |
| rs574321035 | 16:68,344,498 | G/C | — | uncertain significance |
| rs1260707153 | 16:68,344,501 | G/A | — | uncertain significance |
| rs2043497125 | 16:68,344,662 | G/A | — | likely benign |
| rs200733664 | 16:68,344,687 | C/T | — | uncertain significance |
| rs35800405 | 16:68,344,760 | C/T | — | benign |
| rs772301434 | 16:68,344,765 | G/A | — | uncertain significance |
| rs374455092 | 16:68,344,771 | G/A | — | uncertain significance |
| rs751424036 | 16:68,344,784 | T/C | — | uncertain significance |
| rs138348680 | 16:68,344,817 | T/C | — | uncertain significance |
| rs576156259 | 16:68,344,823 | C/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.