LGR6
leucine rich repeat containing G protein-coupled receptor 6
Summary
This gene encodes a member of the leucine-rich repeat-containing subgroup of the G protein-coupled 7-transmembrane protein superfamily. The encoded protein is a glycoprotein hormone receptor with a large N-terminal extracellular domain that contains leucine-rich repeats important for the formation of a horseshoe-shaped interaction motif for ligand binding. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jul 2008]
Known Variants73 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1437113234 | 1:202,163,196 | C/A | — | uncertain significance |
| rs2527456529 | 1:202,163,236 | A/C | — | uncertain significance |
| rs61685000 | 1:202,181,185 | G/A | — | — |
| rs6427943 | 1:202,186,945 | G/C | — | — |
| rs6678914 | 1:202,187,176 | G/A | intron variant | — |
| rs12129456 | 1:202,189,087 | T/A | — | — |
| rs1224929850 | 1:202,197,081 | A/G | — | uncertain significance |
| rs147299721 | 1:202,205,084 | G/A | — | uncertain significance |
| rs1291463656 | 1:202,205,091 | C/T | — | uncertain significance |
| rs749850205 | 1:202,205,106 | C/A | — | uncertain significance |
| rs116047540 | 1:202,232,157 | T/A | intron variant | — |
| rs1271102676 | 1:202,245,436 | G/A | — | uncertain significance |
| rs2528006021 | 1:202,245,444 | G/A | — | uncertain significance |
| rs148637417 | 1:202,245,498 | C/T | — | uncertain significance |
| rs376357186 | 1:202,245,520 | A/G | — | uncertain significance |
| rs142083498 | 1:202,245,595 | G/A | — | uncertain significance |
| rs376700653 | 1:202,245,615 | T/G | — | uncertain significance |
| rs759271868 | 1:202,245,619 | C/T | — | uncertain significance |
| rs77234324 | 1:202,255,325 | G/A | intron variant | — |
| rs705757 | 1:202,260,924 | C/T | — | — |
| rs1667247829 | 1:202,266,636 | A/T | — | likely benign |
| rs1667250902 | 1:202,266,673 | G/A | — | uncertain significance |
| rs788824 | 1:202,267,654 | A/C | — | — |
| rs564376624 | 1:202,272,423 | A/G | — | uncertain significance |
| rs111928234 | 1:202,273,698 | G/A | — | likely benign |
| rs150875603 | 1:202,276,012 | C/T | — | uncertain significance |
| rs201428058 | 1:202,276,045 | C/A | — | uncertain significance |
| rs1653323013 | 1:202,276,492 | C/G | — | uncertain significance |
| rs765693844 | 1:202,278,187 | C/T | — | uncertain significance |
| rs1348471199 | 1:202,278,229 | G/T | — | uncertain significance |
| rs2528245936 | 1:202,278,282 | A/G | — | uncertain significance |
| rs146771876 | 1:202,279,319 | C/G | — | benign |
| rs1015851434 | 1:202,279,431 | G/A | — | uncertain significance |
| rs548446631 | 1:202,283,975 | A/G | — | uncertain significance |
| rs762890791 | 1:202,283,986 | A/C | — | uncertain significance |
| rs749467740 | 1:202,287,108 | T/G | — | uncertain significance |
| rs200345103 | 1:202,287,133 | G/A | — | uncertain significance |
| rs140628646 | 1:202,287,139 | G/A | — | uncertain significance |
| rs1256235993 | 1:202,287,155 | C/T | — | uncertain significance |
| rs2527005412 | 1:202,287,173 | T/G | — | uncertain significance |
| rs143028945 | 1:202,287,187 | G/A | — | uncertain significance |
| rs758614173 | 1:202,287,239 | C/T | — | uncertain significance |
| rs778001193 | 1:202,287,240 | G/A | — | likely benign |
| rs1429135167 | 1:202,287,302 | T/A | — | uncertain significance |
| rs1186765374 | 1:202,287,422 | C/T | — | uncertain significance |
| rs143684053 | 1:202,287,436 | G/A | — | uncertain significance |
| rs763458876 | 1:202,287,442 | G/A | — | uncertain significance |
| rs141252120 | 1:202,287,454 | C/T | — | uncertain significance |
| rs376010617 | 1:202,287,487 | G/A | — | uncertain significance |
| rs758190392 | 1:202,287,491 | G/A | — | uncertain significance |
| rs747233640 | 1:202,287,631 | G/A | — | uncertain significance |
| rs2527014609 | 1:202,287,638 | T/A | — | uncertain significance |
| rs199572358 | 1:202,287,707 | C/T | — | uncertain significance |
| rs111282373 | 1:202,287,708 | G/A | — | likely benign |
| rs1023605716 | 1:202,287,710 | G/A | — | uncertain significance |
| rs144541684 | 1:202,287,727 | G/A | — | uncertain significance |
| rs75303900 | 1:202,287,765 | C/T | — | benign |
| rs2527016649 | 1:202,287,773 | C/T | — | uncertain significance |
| rs145765655 | 1:202,287,818 | C/G | — | uncertain significance |
| rs140358092 | 1:202,287,842 | C/A | — | uncertain significance |
| rs1405802041 | 1:202,287,932 | T/C | — | uncertain significance |
| rs768845813 | 1:202,287,942 | C/A | — | uncertain significance |
| rs2527020348 | 1:202,287,953 | T/C | — | uncertain significance |
| rs374809410 | 1:202,287,962 | G/A | — | uncertain significance |
| rs116127269 | 1:202,287,964 | G/A | — | benign |
| rs151005854 | 1:202,287,995 | C/T | — | uncertain significance |
| rs144773392 | 1:202,288,000 | G/A | — | uncertain significance |
| rs142126765 | 1:202,288,029 | T/C | — | benign |
| rs144407512 | 1:202,288,062 | T/A | — | uncertain significance |
| rs1654406009 | 1:202,288,066 | A/T | — | uncertain significance |
| rs140402059 | 1:202,288,090 | C/T | — | uncertain significance |
| rs151146799 | 1:202,288,091 | G/A | — | likely benign |
| rs267598308 | 1:202,288,099 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.