SERINC2
serine incorporator 2
Summary
Enables phospholipid scramblase activity. Involved in plasma membrane phospholipid scrambling. Located in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants56 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs4478858 | 1:31,883,925 | T/A | — | — |
| rs117944460 | 1:31,886,498 | A/C | regulatory region variant | — |
| rs11589125 | 1:31,894,396 | C/T | regulatory region variant | — |
| rs782394996 | 1:31,896,615 | C/T | — | likely benign |
| rs149433560 | 1:31,896,681 | G/A | — | uncertain significance |
| rs782039097 | 1:31,897,534 | C/T | — | uncertain significance |
| rs2523472827 | 1:31,897,537 | G/C | — | uncertain significance |
| rs148585359 | 1:31,897,552 | G/A | — | uncertain significance |
| rs147664019 | 1:31,897,556 | C/T | — | benign |
| rs782618994 | 1:31,897,569 | G/A | — | likely benign |
| rs112561697 | 1:31,897,587 | G/A | — | benign |
| rs782030981 | 1:31,897,609 | A/G | — | uncertain significance |
| rs782710911 | 1:31,897,612 | G/A | — | uncertain significance |
| rs144622850 | 1:31,897,623 | C/T | — | uncertain significance |
| rs782662561 | 1:31,897,624 | G/A | — | uncertain significance |
| rs782415572 | 1:31,897,654 | T/C | — | uncertain significance |
| rs782101848 | 1:31,897,672 | T/C | — | uncertain significance |
| rs2523474020 | 1:31,897,675 | T/A | — | uncertain significance |
| rs2523474051 | 1:31,897,677 | T/A | — | uncertain significance |
| rs782816945 | 1:31,897,680 | G/A | — | uncertain significance |
| rs183001614 | 1:31,897,692 | C/G | — | likely benign |
| rs572390049 | 1:31,897,701 | C/T | — | uncertain significance |
| rs782482661 | 1:31,897,710 | A/T | — | uncertain significance |
| rs140666908 | 1:31,898,217 | G/A | — | uncertain significance |
| rs1406111453 | 1:31,898,221 | G/A | — | uncertain significance |
| rs371327989 | 1:31,898,241 | G/A | — | uncertain significance |
| rs147315837 | 1:31,898,697 | C/T | — | uncertain significance |
| rs782493926 | 1:31,898,713 | G/C | — | uncertain significance |
| rs139323479 | 1:31,898,730 | G/A | — | uncertain significance |
| rs139893572 | 1:31,898,745 | C/T | — | uncertain significance |
| rs374319929 | 1:31,898,746 | G/A | — | uncertain significance |
| rs146770700 | 1:31,898,757 | G/A | — | uncertain significance |
| rs1641049862 | 1:31,899,503 | C/T | — | uncertain significance |
| rs1211669610 | 1:31,899,548 | G/A | — | uncertain significance |
| rs140789666 | 1:31,899,593 | G/A | — | uncertain significance |
| rs781940917 | 1:31,899,639 | T/C | — | uncertain significance |
| rs2523496988 | 1:31,901,874 | A/C | — | uncertain significance |
| rs782228774 | 1:31,902,258 | C/A | — | uncertain significance |
| rs374259246 | 1:31,902,285 | G/A | — | uncertain significance |
| rs60725155 | 1:31,902,752 | C/T | upstream gene variant | — |
| rs201159674 | 1:31,905,818 | C/T | — | uncertain significance |
| rs147809380 | 1:31,905,819 | G/A | — | uncertain significance |
| rs782746447 | 1:31,905,833 | C/T | — | uncertain significance |
| rs146836894 | 1:31,905,834 | G/A | — | uncertain significance |
| rs376722575 | 1:31,905,884 | G/A | — | uncertain significance |
| rs149573156 | 1:31,905,924 | G/A | — | uncertain significance |
| rs142006438 | 1:31,905,942 | A/G | — | uncertain significance |
| rs139258648 | 1:31,905,947 | G/A | — | uncertain significance |
| rs782500834 | 1:31,905,950 | G/A | — | uncertain significance |
| rs377048384 | 1:31,906,004 | G/A | — | likely benign |
| rs2523530538 | 1:31,906,012 | G/A | — | uncertain significance |
| rs782031627 | 1:31,906,915 | G/A | — | uncertain significance |
| rs11554767 | 1:31,906,941 | G/A | — | likely benign |
| rs151124028 | 1:31,906,948 | G/A | — | uncertain significance |
| rs201298898 | 1:31,907,012 | C/T | — | uncertain significance |
| rs148699108 | 1:31,907,032 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.