IGSF21
immunoglobin superfamily member 21
Summary
This gene encodes a protein which has two immunoglobulin (Ig) domains and is a member of the immunoglobulin superfamily. Proteins in this superfamily are usually found on or in cell membranes and act as receptors in immune response pathways. [provided by RefSeq, Sep 2011]
Known Variants40 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs78116078 | 1:18,434,125 | C/G | regulatory region variant | — |
| rs3767109 | 1:18,434,403 | C/T | regulatory region variant | — |
| rs72944412 | 1:18,487,813 | C/T | intron variant | — |
| rs150336992 | 1:18,554,424 | C/T | — | uncertain significance |
| rs767295536 | 1:18,554,425 | C/A | — | uncertain significance |
| rs371692339 | 1:18,554,442 | G/A | — | uncertain significance |
| rs570910559 | 1:18,616,903 | G/T | — | — |
| rs761315354 | 1:18,618,376 | C/A | — | uncertain significance |
| rs1284876883 | 1:18,618,444 | C/T | — | uncertain significance |
| rs770942594 | 1:18,618,445 | G/T | — | uncertain significance |
| rs748674620 | 1:18,661,393 | G/A | — | uncertain significance |
| rs140409401 | 1:18,688,663 | G/A | — | uncertain significance |
| rs754411603 | 1:18,688,684 | C/A | — | uncertain significance |
| rs766849525 | 1:18,691,717 | G/A | — | uncertain significance |
| rs150815051 | 1:18,691,750 | G/T | — | uncertain significance |
| rs370798003 | 1:18,691,760 | T/C | — | uncertain significance |
| rs774922980 | 1:18,691,802 | G/A | — | uncertain significance |
| rs1180526990 | 1:18,691,814 | G/A | — | uncertain significance |
| rs376868657 | 1:18,691,828 | C/T | — | uncertain significance |
| rs113684099 | 1:18,691,876 | G/A | — | likely benign |
| rs200809740 | 1:18,691,886 | G/A | — | uncertain significance |
| rs746411144 | 1:18,691,898 | C/A | — | uncertain significance |
| rs2355877 | 1:18,691,910 | G/A | — | benign |
| rs141231275 | 1:18,691,919 | G/A | — | likely benign |
| rs140063076 | 1:18,692,014 | A/G | — | uncertain significance |
| rs183577264 | 1:18,692,020 | G/A | — | uncertain significance |
| rs149943630 | 1:18,692,048 | G/A | — | likely benign |
| rs377200558 | 1:18,692,116 | G/C | — | uncertain significance |
| rs151148706 | 1:18,692,173 | C/G | — | uncertain significance |
| rs138302343 | 1:18,702,848 | C/T | missense variant | — |
| rs2521634613 | 1:18,702,851 | G/A | — | uncertain significance |
| rs12076815 | 1:18,703,328 | C/T | — | benign |
| rs141713686 | 1:18,703,354 | G/C | — | uncertain significance |
| rs147858658 | 1:18,703,402 | G/A | — | uncertain significance |
| rs377256717 | 1:18,703,463 | C/T | — | uncertain significance |
| rs144001553 | 1:18,703,479 | C/T | — | benign |
| rs199807152 | 1:18,703,480 | G/A | — | uncertain significance |
| rs376475099 | 1:18,703,899 | T/C | — | uncertain significance |
| rs760730875 | 1:18,703,911 | C/T | — | uncertain significance |
| rs745373657 | 1:18,704,768 | G/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.