PEAR1
platelet endothelial aggregation receptor 1
Summary
PEAR1 is a platelet receptor that signals upon the formation of platelet-platelet contacts independent of platelet activation and secondary to platelet aggregation (Nanda et al., 2005 [PubMed 15851471]).[supplied by OMIM, Mar 2008]
Known Variants73 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs117815664 | 1:156,864,193 | C/T | intron variant | — |
| rs12566888 | 1:156,869,047 | G/A | — | — |
| rs12041331 | 1:156,869,714 | G/A | intron variant | — |
| rs149613819 | 1:156,870,724 | G/A | intron variant | — |
| rs184678074 | 1:156,872,177 | C/T | intron variant | — |
| rs145662369 | 1:156,873,435 | G/T | intron variant | — |
| rs186465653 | 1:156,873,726 | C/T | — | likely benign |
| rs776378615 | 1:156,873,789 | G/A | — | likely benign |
| rs41267433 | 1:156,874,421 | C/G | intron variant | — |
| rs199823758 | 1:156,874,608 | G/A | — | uncertain significance |
| rs139334858 | 1:156,874,628 | A/G | — | uncertain significance |
| rs763663639 | 1:156,875,129 | A/G | — | uncertain significance |
| rs777888743 | 1:156,875,162 | C/T | — | uncertain significance |
| rs772409495 | 1:156,875,184 | A/G | — | likely benign |
| rs143451556 | 1:156,875,193 | A/T | — | uncertain significance |
| rs146185126 | 1:156,876,339 | G/C | intron variant | — |
| rs1354683993 | 1:156,877,407 | A/G | — | uncertain significance |
| rs773757499 | 1:156,877,409 | G/A | — | uncertain significance |
| rs1650495896 | 1:156,877,502 | A/C | — | uncertain significance |
| rs149254521 | 1:156,877,520 | A/G | missense variant | — |
| rs368846340 | 1:156,877,754 | C/A | — | uncertain significance |
| rs145275734 | 1:156,877,782 | G/T | — | benign |
| rs199628333 | 1:156,877,925 | G/T | — | uncertain significance |
| rs767363444 | 1:156,877,955 | A/G | — | uncertain significance |
| rs2525841282 | 1:156,878,102 | C/T | — | uncertain significance |
| rs2525841904 | 1:156,878,126 | G/A | — | uncertain significance |
| rs376228090 | 1:156,878,527 | C/T | — | uncertain significance |
| rs1208320777 | 1:156,878,546 | G/A | — | likely benign |
| rs2525849814 | 1:156,878,584 | C/A | — | uncertain significance |
| rs913658222 | 1:156,878,789 | G/T | — | uncertain significance |
| rs76880868 | 1:156,879,552 | G/C | — | uncertain significance |
| rs3737224 | 1:156,879,580 | C/T | synonymous variant | — |
| rs543273469 | 1:156,879,623 | C/T | — | uncertain significance |
| rs201156993 | 1:156,879,629 | G/A | — | uncertain significance |
| rs147493020 | 1:156,879,633 | T/C | — | likely benign |
| rs1334341513 | 1:156,879,645 | A/G | — | uncertain significance |
| rs757660786 | 1:156,879,647 | A/G | — | uncertain significance |
| rs150001797 | 1:156,879,651 | G/A | — | uncertain significance |
| rs1650847679 | 1:156,879,686 | C/T | — | uncertain significance |
| rs2525868704 | 1:156,879,862 | C/T | — | uncertain significance |
| rs755739282 | 1:156,879,873 | C/T | — | uncertain significance |
| rs200100197 | 1:156,880,031 | C/T | — | uncertain significance |
| rs760024671 | 1:156,880,047 | G/T | — | uncertain significance |
| rs758309003 | 1:156,880,083 | C/A | — | uncertain significance |
| rs369635883 | 1:156,880,146 | G/A | — | uncertain significance |
| rs143342590 | 1:156,880,153 | G/A | — | benign |
| rs766090914 | 1:156,880,463 | C/T | — | uncertain significance |
| rs2525879322 | 1:156,880,466 | T/A | — | uncertain significance |
| rs375455402 | 1:156,880,470 | T/C | — | likely benign |
| rs1570979656 | 1:156,880,524 | A/C | — | uncertain significance |
| rs41273215 | 1:156,881,959 | C/T | intron variant | — |
| rs202159164 | 1:156,882,048 | C/T | — | likely benign |
| rs200307802 | 1:156,882,096 | G/T | — | uncertain significance |
| rs1570989370 | 1:156,882,366 | G/A | — | uncertain significance |
| rs749162792 | 1:156,882,402 | C/T | — | uncertain significance |
| rs532047408 | 1:156,882,589 | C/T | — | uncertain significance |
| rs145923431 | 1:156,882,634 | T/C | — | uncertain significance |
| rs142906924 | 1:156,882,654 | G/A | — | uncertain significance |
| rs113502219 | 1:156,883,029 | C/T | — | benign |
| rs822442 | 1:156,883,215 | C/A | missense variant | benign |
| rs779577377 | 1:156,883,222 | C/T | — | uncertain significance |
| rs746523616 | 1:156,883,223 | G/A | — | uncertain significance |
| rs772202030 | 1:156,883,256 | C/T | — | uncertain significance |
| rs79440685 | 1:156,883,347 | G/A | regulatory region variant | — |
| rs369608309 | 1:156,883,492 | C/T | — | uncertain significance |
| rs767202153 | 1:156,883,522 | A/G | — | uncertain significance |
| rs778091760 | 1:156,883,719 | A/G | — | uncertain significance |
| rs531044292 | 1:156,883,745 | C/T | — | uncertain significance |
| rs371015426 | 1:156,883,794 | C/G | — | uncertain significance |
| rs767278901 | 1:156,883,868 | G/A | — | uncertain significance |
| rs372929905 | 1:156,883,883 | C/G | — | uncertain significance |
| rs190050309 | 1:156,884,475 | C/T | — | uncertain significance |
| rs147546001 | 1:156,884,526 | G/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.