RBP1
retinol binding protein 1
Summary
This gene encodes the carrier protein involved in the transport of retinol (vitamin A alcohol) from the liver storage site to peripheral tissue. Vitamin A is a fat-soluble vitamin necessary for growth, reproduction, differentiation of epithelial tissues, and vision. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2008]
Known Variants109 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs748402108 | 3:139,236,471 | A/T | — | uncertain significance |
| rs1452200423 | 3:139,236,476 | A/T | — | uncertain significance |
| rs528555568 | 3:139,236,501 | C/A | — | uncertain significance |
| rs755878795 | 3:139,236,506 | C/G | — | uncertain significance |
| rs928436654 | 3:139,236,540 | G/A | — | likely benign |
| rs752330304 | 3:139,237,243 | G/C | — | likely benign |
| rs1195593488 | 3:139,237,258 | C/A | — | uncertain significance |
| rs145071297 | 3:139,237,264 | A/G | — | uncertain significance |
| rs1028080103 | 3:139,237,266 | G/C | — | uncertain significance |
| rs144832119 | 3:139,237,272 | C/T | — | likely benign |
| rs367759861 | 3:139,237,273 | T/C | — | uncertain significance |
| rs535310099 | 3:139,237,279 | C/A | — | uncertain significance |
| rs372221405 | 3:139,237,284 | G/A | — | likely benign |
| rs568569893 | 3:139,237,292 | G/A | — | uncertain significance |
| rs753216885 | 3:139,237,293 | G/A | — | likely benign |
| rs770446764 | 3:139,237,301 | C/T | — | uncertain significance |
| rs2107917602 | 3:139,237,302 | A/G | — | likely benign |
| rs376740516 | 3:139,237,303 | C/T | — | uncertain significance |
| rs2472737697 | 3:139,237,312 | T/G | — | uncertain significance |
| rs369475180 | 3:139,237,338 | C/A | — | uncertain significance |
| rs1934806832 | 3:139,237,343 | C/G | — | uncertain significance |
| rs760299969 | 3:139,237,346 | C/A | — | uncertain significance |
| rs148593360 | 3:139,237,347 | G/A | — | benign |
| rs142909523 | 3:139,237,355 | T/C | — | uncertain significance |
| rs1934808141 | 3:139,237,360 | G/A | — | uncertain significance |
| rs1934808243 | 3:139,237,364 | T/C | — | uncertain significance |
| rs968580664 | 3:139,237,368 | C/A | — | likely benign |
| rs295490 | 3:139,241,371 | C/A | — | — |
| rs2071387 | 3:139,257,603 | A/G | — | benign |
| rs759755788 | 3:139,257,606 | T/G | — | likely benign |
| rs1278262027 | 3:139,257,610 | C/G | — | likely benign |
| rs1237076420 | 3:139,257,620 | C/T | — | uncertain significance |
| rs2472783349 | 3:139,257,625 | T/C | — | uncertain significance |
| rs150001856 | 3:139,257,634 | G/A | — | uncertain significance |
| rs140969460 | 3:139,257,645 | C/A | — | uncertain significance |
| rs746373629 | 3:139,257,652 | G/C | — | uncertain significance |
| rs369326542 | 3:139,257,655 | C/T | — | uncertain significance |
| rs1427843267 | 3:139,257,656 | C/A | — | uncertain significance |
| rs1935700055 | 3:139,257,676 | C/T | — | uncertain significance |
| rs747612702 | 3:139,257,683 | G/A | — | likely benign |
| rs373308236 | 3:139,257,692 | G/A | — | likely benign |
| rs1421394926 | 3:139,257,695 | G/C | — | uncertain significance |
| rs2472783874 | 3:139,257,714 | G/A | — | uncertain significance |
| rs1935703899 | 3:139,257,720 | A/G | — | uncertain significance |
| rs34674353 | 3:139,257,727 | T/C | — | benign |
| rs2472783950 | 3:139,257,728 | A/G | — | likely benign |
| rs2107948397 | 3:139,257,741 | T/C | — | uncertain significance |
| rs779352623 | 3:139,257,746 | G/A | — | likely benign |
| rs765575727 | 3:139,257,766 | G/T | — | uncertain significance |
| rs2472784162 | 3:139,257,773 | G/C | — | likely benign |
| rs565159052 | 3:139,257,784 | G/T | — | uncertain significance |
| rs148726176 | 3:139,257,821 | G/C | — | likely benign |
| rs776602131 | 3:139,258,288 | C/T | — | likely benign |
| rs2472786804 | 3:139,258,298 | T/A | — | uncertain significance |
| rs1276325337 | 3:139,258,303 | G/C | — | uncertain significance |
| rs1935741581 | 3:139,258,304 | A/C | — | uncertain significance |
| rs1935742585 | 3:139,258,315 | G/A | — | likely benign |
| rs2472786914 | 3:139,258,318 | C/T | — | likely benign |
| rs759927783 | 3:139,258,321 | C/T | — | likely benign |
| rs2472787011 | 3:139,258,333 | G/T | — | uncertain significance |
| rs1935743974 | 3:139,258,341 | A/G | — | likely benign |
| rs756769759 | 3:139,258,343 | A/G | — | uncertain significance |
| rs1174022918 | 3:139,258,350 | A/C | — | uncertain significance |
| rs1379472115 | 3:139,258,351 | G/A | — | likely benign |
| rs1296620805 | 3:139,258,355 | C/T | — | uncertain significance |
| rs750099202 | 3:139,258,365 | C/A | — | uncertain significance |
| rs576300739 | 3:139,258,369 | T/C | — | benign |
| rs765355546 | 3:139,258,373 | A/G | — | uncertain significance |
| rs1038375447 | 3:139,258,382 | A/T | — | uncertain significance |
| rs368158259 | 3:139,258,390 | G/A | — | likely benign |
| rs545322916 | 3:139,258,394 | C/A | — | uncertain significance |
| rs774611475 | 3:139,258,397 | T/C | — | uncertain significance |
| rs2472787392 | 3:139,258,400 | G/T | — | uncertain significance |
| rs1160288200 | 3:139,258,408 | C/T | — | likely benign |
| rs11549984 | 3:139,258,411 | G/A | — | benign |
| rs2472787558 | 3:139,258,417 | C/T | — | likely benign |
| rs758095834 | 3:139,258,423 | G/A | — | likely benign |
| rs751321164 | 3:139,258,427 | C/A | — | uncertain significance |
| rs1442894304 | 3:139,258,431 | C/T | — | uncertain significance |
| rs1435499551 | 3:139,258,432 | G/A | — | likely benign |
| rs754733560 | 3:139,258,433 | G/A | — | uncertain significance |
| rs781054524 | 3:139,258,434 | G/A | — | uncertain significance |
| rs572591434 | 3:139,258,435 | A/G | — | likely benign |
| rs756233491 | 3:139,258,436 | C/T | — | uncertain significance |
| rs1010119517 | 3:139,258,440 | G/A | — | uncertain significance |
| rs777799194 | 3:139,258,451 | C/G | — | uncertain significance |
| rs1165805911 | 3:139,258,462 | G/C | — | uncertain significance |
| rs774576614 | 3:139,258,467 | C/T | — | uncertain significance |
| rs1464580517 | 3:139,258,469 | G/T | — | uncertain significance |
| rs1397670366 | 3:139,258,473 | G/A | — | uncertain significance |
| rs979108517 | 3:139,258,496 | A/T | — | uncertain significance |
| rs1277098745 | 3:139,258,497 | G/A | — | likely benign |
| rs761245937 | 3:139,258,502 | C/A | — | uncertain significance |
| rs2071386 | 3:139,258,508 | G/A | — | benign |
| rs772867674 | 3:139,258,515 | C/T | — | uncertain significance |
| rs561177753 | 3:139,258,516 | G/A | — | likely benign |
| rs1476332666 | 3:139,258,524 | G/A | — | uncertain significance |
| rs530222014 | 3:139,258,529 | C/G | — | uncertain significance |
| rs754785993 | 3:139,258,534 | G/C | — | likely benign |
| rs1477094090 | 3:139,258,536 | G/A | — | uncertain significance |
Showing 100 of 109 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.