MFSD2B
MFSD2 lysolipid transporter B, sphingolipid
Summary
Enables sphingolipid transporter activity. Involved in lipid transport. Is active in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants47 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs72781671 | 2:24,231,123 | A/G | downstream gene variant | — |
| rs576269656 | 2:24,232,977 | C/T | — | uncertain significance |
| rs543378642 | 2:24,232,987 | A/G | — | likely benign |
| rs565084908 | 2:24,233,030 | C/G | — | uncertain significance |
| rs780620360 | 2:24,233,037 | C/A | — | uncertain significance |
| rs2339936 | 2:24,235,047 | C/G | — | — |
| rs534559168 | 2:24,236,170 | C/G | — | uncertain significance |
| rs11887523 | 2:24,236,236 | G/C | missense variant | — |
| rs767978286 | 2:24,236,264 | T/G | — | uncertain significance |
| rs56036119 | 2:24,236,496 | T/C | — | — |
| rs72781679 | 2:24,237,712 | G/A | intron variant | — |
| rs72781680 | 2:24,238,928 | C/T | regulatory region variant | — |
| rs375751768 | 2:24,239,138 | G/A | — | uncertain significance |
| rs200036575 | 2:24,239,812 | T/A | — | uncertain significance |
| rs765040513 | 2:24,240,178 | C/G | — | uncertain significance |
| rs774723440 | 2:24,240,220 | C/T | — | uncertain significance |
| rs895534026 | 2:24,240,228 | G/T | — | uncertain significance |
| rs369613796 | 2:24,240,369 | G/A | — | uncertain significance |
| rs200479309 | 2:24,240,390 | G/A | — | uncertain significance |
| rs1302626581 | 2:24,240,393 | G/A | — | uncertain significance |
| rs769192324 | 2:24,240,398 | C/A | — | uncertain significance |
| rs747126152 | 2:24,244,525 | T/C | — | uncertain significance |
| rs1163388210 | 2:24,244,537 | C/T | — | uncertain significance |
| rs201522941 | 2:24,244,545 | G/A | — | uncertain significance |
| rs768709238 | 2:24,244,602 | C/T | — | uncertain significance |
| rs1386097970 | 2:24,245,324 | C/G | — | uncertain significance |
| rs138903557 | 2:24,245,713 | C/G | missense variant | — |
| rs371261417 | 2:24,245,753 | C/T | — | likely benign |
| rs765760208 | 2:24,246,009 | C/T | — | uncertain significance |
| rs370067208 | 2:24,246,060 | G/A | — | uncertain significance |
| rs754893160 | 2:24,246,469 | G/A | — | uncertain significance |
| rs765739052 | 2:24,246,485 | A/C | — | uncertain significance |
| rs200112704 | 2:24,246,518 | C/A | — | uncertain significance |
| rs545973973 | 2:24,246,565 | T/C | — | uncertain significance |
| rs1662897455 | 2:24,246,976 | A/G | — | uncertain significance |
| rs201963647 | 2:24,246,987 | G/T | — | uncertain significance |
| rs372166240 | 2:24,246,993 | A/G | — | uncertain significance |
| rs768971294 | 2:24,246,999 | G/A | — | uncertain significance |
| rs751215494 | 2:24,247,038 | G/A | — | uncertain significance |
| rs747170388 | 2:24,247,060 | T/C | — | uncertain significance |
| rs762582329 | 2:24,247,086 | G/A | — | uncertain significance |
| rs986045982 | 2:24,247,098 | A/G | — | uncertain significance |
| rs758480146 | 2:24,247,111 | G/C | — | uncertain significance |
| rs373852333 | 2:24,247,137 | C/T | — | uncertain significance |
| rs201093645 | 2:24,247,138 | G/A | — | uncertain significance |
| rs7561273 | 2:24,247,514 | A/C | — | — |
| rs7561675 | 2:24,247,818 | A/C | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.