ITGBL1
integrin subunit beta like 1
Summary
This gene encodes a beta integrin-related protein that is a member of the EGF-like protein family. The encoded protein contains integrin-like cysteine-rich repeats. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2012]
Known Variants38 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1475634367 | 13:102,105,225 | C/T | — | uncertain significance |
| rs982820653 | 13:102,106,283 | C/G | — | uncertain significance |
| rs2548662005 | 13:102,106,316 | G/A | — | uncertain significance |
| rs759374278 | 13:102,106,326 | A/G | — | uncertain significance |
| rs775199348 | 13:102,106,329 | G/A | — | uncertain significance |
| rs1326478098 | 13:102,106,331 | C/T | — | uncertain significance |
| rs938164927 | 13:102,106,332 | G/T | — | uncertain significance |
| rs150532305 | 13:102,106,438 | G/C | — | benign |
| rs9582490 | 13:102,127,680 | T/C | intron variant | — |
| rs1335587 | 13:102,145,560 | C/G | — | — |
| rs185293941 | 13:102,202,067 | G/T | intron variant | — |
| rs62637618 | 13:102,220,050 | G/A | — | benign |
| rs199728594 | 13:102,220,121 | A/G | — | uncertain significance |
| rs2050205620 | 13:102,220,141 | G/T | — | uncertain significance |
| rs766447430 | 13:102,220,178 | A/T | — | uncertain significance |
| rs9557704 | 13:102,227,495 | A/T | intron variant | — |
| rs2548761515 | 13:102,231,647 | A/G | — | uncertain significance |
| rs755776332 | 13:102,231,648 | G/T | — | uncertain significance |
| rs2548761723 | 13:102,231,716 | T/A | — | uncertain significance |
| rs2548766797 | 13:102,235,581 | G/A | — | uncertain significance |
| rs1158852212 | 13:102,235,623 | G/A | — | uncertain significance |
| rs750974072 | 13:102,235,659 | G/A | — | uncertain significance |
| rs374036212 | 13:102,250,539 | A/G | — | uncertain significance |
| rs562841426 | 13:102,250,561 | G/C | — | uncertain significance |
| rs751202946 | 13:102,344,965 | A/G | — | uncertain significance |
| rs370206931 | 13:102,344,982 | C/T | — | uncertain significance |
| rs762946447 | 13:102,345,019 | G/A | — | uncertain significance |
| rs72659186 | 13:102,347,723 | C/A | intron variant | — |
| rs373082645 | 13:102,359,111 | G/A | — | uncertain significance |
| rs62637619 | 13:102,359,175 | C/T | — | benign |
| rs62637620 | 13:102,359,176 | G/A | — | benign |
| rs761611322 | 13:102,359,177 | C/T | — | uncertain significance |
| rs149770736 | 13:102,359,178 | G/A | — | uncertain significance |
| rs753390115 | 13:102,359,193 | C/T | — | uncertain significance |
| rs146829108 | 13:102,359,244 | C/T | — | uncertain significance |
| rs754090600 | 13:102,366,809 | G/A | — | uncertain significance |
| rs770748136 | 13:102,366,874 | G/A | — | uncertain significance |
| rs144243522 | 13:102,367,975 | G/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.