SCARB1
scavenger receptor class B member 1
Summary
The protein encoded by this gene is a plasma membrane receptor for high density lipoprotein cholesterol (HDL). The encoded protein mediates cholesterol transfer to and from HDL. In addition, this protein is a receptor for hepatitis C virus glycoprotein E2 and facilitates cell entry by the virus, SARS-CoV2. [provided by RefSeq, Oct 2021]
Known Variants164 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1672877 | 12:125,261,208 | T/G | downstream gene variant | — |
| rs838880 | 12:125,261,593 | C/A | — | — |
| rs701103 | 12:125,263,039 | C/T | — | benign |
| rs3825140 | 12:125,263,061 | C/T | — | benign |
| rs568188228 | 12:125,263,118 | G/A | — | likely benign |
| rs747155 | 12:125,263,244 | G/A | — | benign |
| rs188375019 | 12:125,263,275 | G/A | — | likely benign |
| rs921919 | 12:125,265,201 | G/A | regulatory region variant | — |
| rs75446635 | 12:125,267,151 | C/T | — | likely benign |
| rs2548093315 | 12:125,267,234 | G/C | — | uncertain significance |
| rs764880118 | 12:125,267,255 | A/G | — | uncertain significance |
| rs1233229414 | 12:125,267,295 | C/T | — | likely benign |
| rs576636212 | 12:125,267,329 | C/A | — | uncertain significance |
| rs772988886 | 12:125,267,352 | T/G | — | uncertain significance |
| rs2135526034 | 12:125,267,373 | G/A | — | likely benign |
| rs746211975 | 12:125,267,374 | C/T | — | likely benign |
| rs838895 | 12:125,269,692 | G/A | — | — |
| rs75289200 | 12:125,270,729 | A/G | — | likely benign |
| rs2293440 | 12:125,270,773 | A/G | — | benign |
| rs764459209 | 12:125,270,945 | G/A | — | likely benign |
| rs528859014 | 12:125,270,966 | G/A | — | likely benign |
| rs2135540455 | 12:125,270,971 | G/A | — | uncertain significance |
| rs2135540474 | 12:125,270,974 | C/G | — | uncertain significance |
| rs200718786 | 12:125,271,047 | G/A | — | likely benign |
| rs908650658 | 12:125,271,053 | A/G | — | likely benign |
| rs775724383 | 12:125,271,059 | C/T | — | likely benign |
| rs838897 | 12:125,271,090 | G/C | — | benign |
| rs2293439 | 12:125,271,101 | A/C | — | benign |
| rs838898 | 12:125,271,118 | C/T | — | benign |
| rs2272310 | 12:125,271,678 | C/T | — | benign |
| rs202096858 | 12:125,271,941 | C/T | — | likely benign |
| rs757231326 | 12:125,271,962 | C/T | — | uncertain significance |
| rs149597476 | 12:125,271,996 | C/T | — | likely benign |
| rs371132142 | 12:125,272,007 | G/T | — | uncertain significance |
| rs9919713 | 12:125,272,763 | A/G | — | — |
| rs12580323 | 12:125,279,661 | C/T | — | likely benign |
| rs202048724 | 12:125,279,723 | C/T | — | benign |
| rs751100225 | 12:125,279,745 | T/C | — | uncertain significance |
| rs757101173 | 12:125,279,751 | C/T | — | uncertain significance |
| rs748231262 | 12:125,279,810 | G/A | — | uncertain significance |
| rs773699924 | 12:125,279,818 | C/T | — | likely benign |
| rs10396210 | 12:125,279,821 | C/T | — | benign |
| rs1672879 | 12:125,281,102 | G/T | intron variant | — |
| rs1672907 | 12:125,283,403 | G/A | — | — |
| rs838915 | 12:125,284,597 | G/T | — | benign |
| rs370318228 | 12:125,284,667 | C/T | — | uncertain significance |
| rs74830677 | 12:125,284,671 | G/A | missense variant | pathogenic |
| rs369653232 | 12:125,284,676 | G/A | — | likely benign |
| rs2548130566 | 12:125,284,699 | C/T | — | uncertain significance |
| rs372663606 | 12:125,284,742 | C/T | — | likely benign |
| rs5888 | 12:125,284,748 | A/G | synonymous variant | benign |
| rs146394799 | 12:125,284,757 | G/A | — | likely benign |
| rs758629966 | 12:125,284,760 | G/T | — | uncertain significance |
| rs2135596186 | 12:125,284,765 | G/T | — | uncertain significance |
| rs838913 | 12:125,285,953 | T/A | — | — |
| rs838912 | 12:125,286,037 | T/G | — | — |
| rs3782287 | 12:125,289,265 | G/C | — | — |
| rs561960354 | 12:125,292,308 | G/A | — | likely benign |
| rs139784395 | 12:125,292,325 | C/T | — | likely benign |
| rs150728540 | 12:125,292,360 | C/A | — | uncertain significance |
| rs2548143591 | 12:125,292,369 | G/T | — | uncertain significance |
| rs140581411 | 12:125,292,383 | C/T | — | benign |
| rs756256849 | 12:125,292,386 | G/A | — | likely benign |
| rs5892 | 12:125,292,413 | G/A | — | benign |
| rs387906791 | 12:125,292,427 | G/A | — | association |
| rs61762483 | 12:125,292,653 | C/T | — | likely benign |
| rs838902 | 12:125,292,675 | T/C | — | benign |
| rs200952914 | 12:125,294,700 | C/T | — | benign |
| rs547400313 | 12:125,294,731 | C/T | — | benign |
| rs1469583262 | 12:125,294,732 | G/A | — | uncertain significance |
| rs759334503 | 12:125,294,749 | C/T | — | likely benign |
| rs771694795 | 12:125,294,788 | A/G | — | likely benign |
| rs201357313 | 12:125,294,817 | C/A | — | uncertain significance |
| rs201068540 | 12:125,294,837 | T/G | — | pathogenic |
| rs188756468 | 12:125,294,844 | A/G | — | likely benign |
| rs1383308986 | 12:125,294,848 | A/T | — | uncertain significance |
| rs61762481 | 12:125,295,028 | C/T | — | benign |
| rs112371713 | 12:125,296,161 | C/T | — | benign |
| rs59809936 | 12:125,296,361 | C/T | — | benign |
| rs61932577 | 12:125,296,362 | A/G | — | benign |
| rs769174348 | 12:125,296,407 | G/A | — | likely benign |
| rs774768995 | 12:125,296,408 | C/T | — | likely benign |
| rs201977189 | 12:125,296,427 | C/T | — | uncertain significance |
| rs757116603 | 12:125,296,455 | G/C | — | uncertain significance |
| rs10396213 | 12:125,296,457 | T/C | — | likely benign |
| rs1010535276 | 12:125,296,483 | G/A | — | uncertain significance |
| rs780989061 | 12:125,296,499 | C/T | — | uncertain significance |
| rs113910315 | 12:125,296,525 | A/C | — | benign |
| rs77740046 | 12:125,296,564 | G/A | — | benign |
| rs114072582 | 12:125,296,704 | G/A | — | likely benign |
| rs75551670 | 12:125,296,714 | G/A | — | benign |
| rs12297430 | 12:125,296,750 | G/A | — | benign |
| rs11057820 | 12:125,296,964 | C/T | intron variant | — |
| rs138600805 | 12:125,298,733 | C/T | — | likely benign |
| rs766081187 | 12:125,298,744 | G/A | — | uncertain significance |
| rs2548153662 | 12:125,298,837 | A/G | — | uncertain significance |
| rs187831231 | 12:125,298,855 | T/C | — | uncertain significance |
| rs367669186 | 12:125,298,858 | G/A | — | uncertain significance |
| rs5889 | 12:125,298,877 | G/A | — | benign |
| rs199588922 | 12:125,298,879 | C/T | — | uncertain significance |
Showing 100 of 164 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.