SLCO2A1
solute carrier organic anion transporter family member 2A1
Summary
This gene encodes a prostaglandin transporter that is a member of the 12-membrane-spanning superfamily of transporters. The encoded protein may be involved in mediating the uptake and clearance of prostaglandins in numerous tissues. [provided by RefSeq, Dec 2011]
Known Variants258 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs149529847 | 3:133,653,558 | C/G | — | uncertain significance |
| rs72978391 | 3:133,653,566 | G/A | — | benign |
| rs138783423 | 3:133,653,572 | C/T | — | likely benign |
| rs200078271 | 3:133,653,584 | G/A | — | benign |
| rs757611356 | 3:133,653,590 | C/T | — | likely benign |
| rs2530950335 | 3:133,653,616 | T/A | — | uncertain significance |
| rs1933226184 | 3:133,653,638 | G/C | — | likely benign |
| rs748877837 | 3:133,653,644 | C/T | — | likely benign |
| rs148426132 | 3:133,653,645 | G/A | — | uncertain significance |
| rs200115070 | 3:133,653,652 | A/G | — | uncertain significance |
| rs141699948 | 3:133,653,662 | C/T | — | likely benign |
| rs1172803733 | 3:133,653,676 | T/A | — | uncertain significance |
| rs375564210 | 3:133,653,685 | G/A | — | likely benign |
| rs201960310 | 3:133,653,688 | G/A | — | likely benign |
| rs376718231 | 3:133,653,689 | A/C | — | likely benign |
| rs568073304 | 3:133,653,785 | T/C | — | uncertain significance |
| rs1228962945 | 3:133,654,607 | T/A | — | likely benign |
| rs2108035365 | 3:133,654,611 | C/T | — | likely benign |
| rs2108035368 | 3:133,654,617 | C/T | — | pathogenic |
| rs527244554 | 3:133,654,620 | G/A | — | likely benign |
| rs187907881 | 3:133,654,624 | C/G | — | uncertain significance |
| rs776813259 | 3:133,654,625 | G/A | stop gained | pathogenic |
| rs2530952440 | 3:133,654,633 | T/A | — | uncertain significance |
| rs762008407 | 3:133,654,634 | C/T | — | uncertain significance |
| rs117837593 | 3:133,654,635 | G/A | — | benign |
| rs150503809 | 3:133,654,649 | C/T | — | uncertain significance |
| rs751921800 | 3:133,654,650 | G/A | — | likely benign |
| rs200281986 | 3:133,654,660 | C/T | — | uncertain significance |
| rs768030732 | 3:133,654,661 | G/A | — | pathogenic |
| rs376867255 | 3:133,654,665 | C/T | — | likely benign |
| rs149850080 | 3:133,654,677 | C/A | — | likely benign |
| rs144464929 | 3:133,654,687 | C/T | — | likely benign |
| rs201986457 | 3:133,654,690 | A/C | — | uncertain significance |
| rs1933256338 | 3:133,654,704 | A/T | — | likely benign |
| rs2108035460 | 3:133,654,714 | C/A | — | uncertain significance |
| rs773226359 | 3:133,654,746 | A/G | — | likely benign |
| rs766536436 | 3:133,654,751 | G/T | — | likely benign |
| rs7616492 | 3:133,654,846 | G/A | — | benign |
| rs4502579 | 3:133,655,001 | G/A | — | benign |
| rs774522730 | 3:133,657,267 | A/G | — | uncertain significance |
| rs565486627 | 3:133,657,291 | A/G | — | likely benign |
| rs1933329681 | 3:133,657,295 | C/G | — | pathogenic |
| rs1177054873 | 3:133,657,303 | C/T | — | pathogenic |
| rs199895359 | 3:133,657,306 | T/C | — | likely benign |
| rs376107710 | 3:133,657,354 | G/C | — | likely benign |
| rs10935089 | 3:133,657,632 | C/T | — | benign |
| rs148769636 | 3:133,658,965 | C/T | — | — |
| rs3923834 | 3:133,661,352 | G/T | — | benign |
| rs200626311 | 3:133,661,432 | A/G | — | benign |
| rs1201137598 | 3:133,661,441 | C/G | — | likely benign |
| rs777114537 | 3:133,661,443 | A/G | — | likely pathogenic |
| rs770432752 | 3:133,661,449 | C/T | — | uncertain significance |
| rs566240756 | 3:133,661,450 | G/A | — | conflicting classifications of pathogenicity |
| rs140206661 | 3:133,661,459 | T/C | — | uncertain significance |
| rs145832999 | 3:133,661,493 | C/G | — | likely benign |
| rs148949815 | 3:133,661,501 | C/T | — | uncertain significance |
| rs747190330 | 3:133,661,502 | G/A | — | likely benign |
| rs376344584 | 3:133,661,523 | C/T | — | likely benign |
| rs773837399 | 3:133,661,524 | G/A | — | uncertain significance |
| rs749871960 | 3:133,661,532 | G/A | — | likely benign |
| rs771480419 | 3:133,661,537 | G/C | — | uncertain significance |
| rs143723313 | 3:133,661,540 | C/G | — | uncertain significance |
| rs146062143 | 3:133,661,558 | A/T | — | likely benign |
| rs200364668 | 3:133,661,565 | C/A | — | conflicting classifications of pathogenicity |
| rs138923414 | 3:133,661,576 | C/T | — | conflicting classifications of pathogenicity |
| rs142933499 | 3:133,661,577 | G/A | — | likely benign |
| rs201991746 | 3:133,661,585 | C/T | — | likely benign |
| rs1033195776 | 3:133,661,586 | G/A | — | likely benign |
| rs746561186 | 3:133,661,598 | G/A | — | likely benign |
| rs750003675 | 3:133,661,621 | G/A | — | likely benign |
| rs9818609 | 3:133,663,681 | A/G | — | benign |
| rs2530970295 | 3:133,663,938 | C/G | — | pathogenic |
| rs772939316 | 3:133,663,960 | G/A | — | likely benign |
| rs375938553 | 3:133,663,966 | G/T | — | conflicting classifications of pathogenicity |
| rs574080271 | 3:133,663,983 | C/T | — | uncertain significance |
| rs150345667 | 3:133,664,015 | T/C | — | likely benign |
| rs2530970477 | 3:133,664,018 | T/C | — | uncertain significance |
| rs748955819 | 3:133,664,027 | A/G | — | uncertain significance |
| rs892909504 | 3:133,664,028 | C/A | — | pathogenic |
| rs199835859 | 3:133,664,029 | C/G | — | likely benign |
| rs745763957 | 3:133,664,030 | G/C | — | uncertain significance |
| rs373457618 | 3:133,664,053 | C/T | — | likely benign |
| rs2108040441 | 3:133,664,055 | A/G | — | uncertain significance |
| rs146970901 | 3:133,664,067 | G/A | — | likely benign |
| rs147644142 | 3:133,664,084 | G/A | — | uncertain significance |
| rs141527637 | 3:133,664,101 | T/C | — | likely benign |
| rs772035055 | 3:133,664,103 | T/C | — | uncertain significance |
| rs768777405 | 3:133,664,120 | G/A | — | likely benign |
| rs185512148 | 3:133,664,124 | C/T | — | likely benign |
| rs2530973394 | 3:133,666,080 | C/G | — | likely benign |
| rs146195307 | 3:133,666,104 | G/C | — | uncertain significance |
| rs530021473 | 3:133,666,107 | G/A | — | benign |
| rs750150056 | 3:133,666,113 | C/A | — | uncertain significance |
| rs377719582 | 3:133,666,116 | C/T | — | uncertain significance |
| rs746875740 | 3:133,666,117 | G/A | — | likely benign |
| rs387907295 | 3:133,666,136 | C/A | missense variant | pathogenic |
| rs34566804 | 3:133,666,152 | A/G | — | benign |
| rs916048612 | 3:133,666,190 | G/A | — | uncertain significance |
| rs532222872 | 3:133,666,199 | C/T | — | uncertain significance |
| rs34550074 | 3:133,666,209 | T/C | — | benign |
Showing 100 of 258 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.