SCARF1
scavenger receptor class F member 1
Summary
The protein encoded by this gene is a scavenger receptor that is expressed in endothelial cells. It regulates the uptake of chemically modified low density lipoproteins, including acetylated low density lipoprotein (Ac-LDL), and it may be involved in atherogenesis. This gene is regulated by the transcription factors ZNF444/EZF-2 and SP1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2013]
Known Variants61 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs142148792 | 17:1,538,083 | A/G | — | benign |
| rs1481444267 | 17:1,538,139 | C/G | — | uncertain significance |
| rs139315899 | 17:1,538,147 | G/C | — | uncertain significance |
| rs1023921534 | 17:1,538,243 | G/A | — | likely benign |
| rs374751391 | 17:1,538,248 | G/A | — | uncertain significance |
| rs770566724 | 17:1,538,281 | T/C | — | likely benign |
| rs2543655670 | 17:1,538,311 | A/G | — | uncertain significance |
| rs1291541706 | 17:1,538,312 | G/A | — | uncertain significance |
| rs372315017 | 17:1,538,318 | G/A | — | uncertain significance |
| rs750671486 | 17:1,538,333 | G/A | — | uncertain significance |
| rs370443375 | 17:1,538,350 | G/A | — | uncertain significance |
| rs1396336432 | 17:1,538,374 | A/C | — | uncertain significance |
| rs375338375 | 17:1,538,375 | C/A | — | uncertain significance |
| rs771888714 | 17:1,538,376 | C/G | — | uncertain significance |
| rs1194559123 | 17:1,538,414 | G/A | — | uncertain significance |
| rs943832555 | 17:1,538,540 | T/G | — | uncertain significance |
| rs761516517 | 17:1,538,564 | G/A | — | uncertain significance |
| rs3744644 | 17:1,538,628 | C/G | missense variant | — |
| rs528173063 | 17:1,538,656 | C/T | — | likely benign |
| rs760501209 | 17:1,538,683 | C/G | — | uncertain significance |
| rs1909469582 | 17:1,538,737 | C/T | — | uncertain significance |
| rs143320036 | 17:1,538,749 | G/A | — | uncertain significance |
| rs369553841 | 17:1,538,765 | C/G | — | uncertain significance |
| rs200063321 | 17:1,538,779 | G/A | — | uncertain significance |
| rs1909485567 | 17:1,538,843 | C/T | — | uncertain significance |
| rs1909597840 | 17:1,540,063 | A/T | — | uncertain significance |
| rs754727687 | 17:1,540,078 | C/T | — | uncertain significance |
| rs145590674 | 17:1,540,091 | G/A | — | likely benign |
| rs749226351 | 17:1,540,102 | G/A | — | uncertain significance |
| rs867668544 | 17:1,540,135 | G/A | — | uncertain significance |
| rs1909631166 | 17:1,540,327 | C/T | — | uncertain significance |
| rs369633804 | 17:1,540,334 | C/T | — | uncertain significance |
| rs1347567281 | 17:1,542,118 | C/T | — | uncertain significance |
| rs758403808 | 17:1,542,209 | G/A | — | uncertain significance |
| rs2543670433 | 17:1,542,953 | A/G | — | uncertain significance |
| rs529850788 | 17:1,543,019 | G/C | — | uncertain significance |
| rs148329015 | 17:1,543,222 | C/T | — | uncertain significance |
| rs201337336 | 17:1,543,245 | G/A | — | uncertain significance |
| rs2543671747 | 17:1,543,275 | G/A | — | uncertain significance |
| rs202081378 | 17:1,543,770 | G/A | — | uncertain significance |
| rs142937472 | 17:1,543,805 | C/T | — | uncertain significance |
| rs200107670 | 17:1,543,880 | G/A | — | uncertain significance |
| rs2543674171 | 17:1,543,902 | A/G | — | uncertain significance |
| rs748661614 | 17:1,543,953 | G/A | — | uncertain significance |
| rs2543682353 | 17:1,546,806 | G/A | — | uncertain significance |
| rs917379871 | 17:1,546,809 | G/C | — | uncertain significance |
| rs1910282718 | 17:1,546,928 | G/A | — | uncertain significance |
| rs2543683403 | 17:1,546,970 | C/A | — | uncertain significance |
| rs989920281 | 17:1,546,994 | G/T | — | uncertain significance |
| rs1489133707 | 17:1,547,060 | G/A | — | uncertain significance |
| rs1213856296 | 17:1,547,072 | G/A | — | uncertain significance |
| rs1286791365 | 17:1,547,103 | C/T | — | uncertain significance |
| rs983469924 | 17:1,547,120 | C/T | — | uncertain significance |
| rs908777248 | 17:1,547,145 | G/T | — | uncertain significance |
| rs931724063 | 17:1,547,186 | G/T | — | uncertain significance |
| rs1233545890 | 17:1,547,255 | G/A | — | uncertain significance |
| rs200821645 | 17:1,548,166 | C/T | — | uncertain significance |
| rs772819223 | 17:1,548,214 | G/A | — | likely benign |
| rs763555736 | 17:1,548,532 | G/A | — | uncertain significance |
| rs1910474049 | 17:1,548,903 | C/T | — | uncertain significance |
| rs143791504 | 17:1,548,908 | G/A | — | benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.