LOC400499
apolipoprotein lipid transfer particle homolog
Known Variants14 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1232165169 | 16:11,501,101 | C/T | — | likely benign |
| rs576805773 | 16:11,511,519 | C/T | — | likely benign |
| rs757047691 | 16:11,511,573 | G/A | — | likely benign |
| rs1036764893 | 16:11,519,012 | C/T | — | likely benign |
| rs1333685956 | 16:11,519,207 | G/A | — | likely benign |
| rs4129933 | 16:11,528,893 | C/A | intron variant | — |
| rs560208862 | 16:11,533,420 | G/A | — | likely benign |
| rs116544709 | 16:11,536,769 | C/T | intron variant | — |
| rs184584020 | 16:11,542,857 | C/T | — | likely benign |
| rs145058041 | 16:11,542,955 | T/C | — | likely benign |
| rs74735089 | 16:11,544,950 | G/A | intron variant | — |
| rs911755827 | 16:11,554,390 | G/A | — | likely benign |
| rs2061021835 | 16:11,570,661 | A/G | — | likely benign |
| rs777265862 | 16:11,609,904 | G/T | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.