ADGRG6

adhesion G protein-coupled receptor G6

Summary

This gene, which is upregulated in human umbilical vein endothelial cells, encodes a G protein-coupled receptor. Variations in this gene can affect a person's stature. Multiple transcript variants encoding different proteins have been found for this gene. [provided by RefSeq, Mar 2009]

Known Variants169 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs113040504	6:142,622,823	A/G	—	benign
rs74857485	6:142,622,955	A/G	—	benign
rs80265926	6:142,622,958	C/T	—	benign
rs113297468	6:142,623,043	T/C	—	benign
rs73576330	6:142,623,153	T/G	—	benign
rs77043049	6:142,623,201	C/T	—	benign
rs112490548	6:142,623,226	G/A	—	benign
rs58392058	6:142,623,228	C/T	—	benign
rs115240560	6:142,623,647	A/G	—	benign
rs28461686	6:142,630,658	A/G	—	benign
rs749355583	6:142,630,697	C/T	stop gained	pathogenic
rs1217873370	6:142,630,712	C/T	—	uncertain significance
rs763677717	6:142,630,740	T/C	—	uncertain significance
rs145672534	6:142,630,763	A/G	—	likely benign
rs12189801	6:142,641,606	T/C	intron variant	—
rs1418201	6:142,648,056	A/C	—	—
rs9389984	6:142,652,344	C/G	—	—
rs9403380	6:142,652,416	T/A	—	—
rs9389985	6:142,653,898	A/C	—	—
rs2039987	6:142,655,490	A/G	—	—
rs7741741	6:142,655,801	T/A	regulatory region variant	—
rs191441541	6:142,659,182	G/A	intron variant	—
rs74967581	6:142,663,848	C/T	intron variant	—
rs7774095	6:142,670,862	C/A	regulatory region variant	—
rs140746093	6:142,672,851	A/G	intron variant	—
rs142016511	6:142,678,675	G/T	intron variant	—
rs6570507	6:142,679,572	G/A	intron variant	—
rs2114851754	6:142,688,750	G/A	—	uncertain significance
rs202040079	6:142,688,804	A/G	—	conflicting classifications of pathogenicity
rs116955726	6:142,688,811	C/T	—	benign
rs192254609	6:142,688,817	G/A	—	uncertain significance
rs35699755	6:142,688,827	C/T	—	benign
rs766540867	6:142,688,841	A/G	—	uncertain significance
rs1781021909	6:142,688,907	A/G	—	uncertain significance
rs2483155213	6:142,688,934	G/A	—	uncertain significance
rs140723393	6:142,688,956	A/G	—	likely benign
rs17280293	6:142,688,969	A/G	—	benign
rs75679810	6:142,689,042	T/A	—	benign
rs778631441	6:142,691,312	G/A	—	uncertain significance
rs2483175681	6:142,691,368	A/G	—	likely benign
rs750228405	6:142,691,436	T/C	—	uncertain significance
rs375861051	6:142,691,443	T/A	—	benign
rs2483176675	6:142,691,459	A/T	—	uncertain significance
rs11155242	6:142,691,549	A/C	missense variant	—
rs201621259	6:142,691,569	A/C	—	likely benign
rs199531526	6:142,691,613	A/G	—	uncertain significance
rs111589388	6:142,691,655	G/C	—	likely benign
rs762744259	6:142,691,657	G/A	—	uncertain significance
rs201497641	6:142,691,777	G/T	—	benign
rs201582584	6:142,691,827	C/G	—	likely benign
rs145304917	6:142,691,861	G/A	—	uncertain significance
rs200437948	6:142,691,874	A/T	—	likely benign
rs745695876	6:142,691,920	C/G	—	uncertain significance
rs9496354	6:142,692,078	C/A	—	benign
rs77898429	6:142,695,018	C/T	—	—
rs6909857	6:142,701,158	A/G	intron variant	—
rs376452752	6:142,703,127	G/T	—	uncertain significance
rs2143390	6:142,703,137	C/T	—	benign
rs201373020	6:142,703,165	C/T	—	likely benign
rs6922607	6:142,703,483	A/G	intron variant	—
rs4896582	6:142,703,877	G/A	intron variant	—
rs182651892	6:142,704,947	C/A	—	uncertain significance
rs41289839	6:142,705,070	G/A	—	benign
rs6937121	6:142,707,133	T/A	—	—
rs534089695	6:142,711,410	G/A	—	uncertain significance
rs201905626	6:142,711,468	G/T	—	uncertain significance
rs376357580	6:142,714,089	A/G	—	uncertain significance
rs117541893	6:142,714,117	G/A	—	benign
rs144911800	6:142,714,127	G/A	—	likely benign
rs774026696	6:142,714,131	A/G	—	uncertain significance
rs1277932989	6:142,715,024	T/C	—	likely benign
rs926862737	6:142,715,097	T/A	—	likely pathogenic
rs17071756	6:142,715,195	T/C	—	benign
rs6570509	6:142,716,286	G/T	intron variant	—
rs78508646	6:142,718,625	T/C	—	benign
rs1046610929	6:142,718,753	G/T	—	uncertain significance
rs906779118	6:142,718,754	G/T	—	uncertain significance
rs989946	6:142,718,801	G/A	—	benign
rs372053605	6:142,718,843	G/T	—	uncertain significance
rs202032349	6:142,718,850	G/A	—	uncertain significance
rs1237575614	6:142,718,853	G/A	—	uncertain significance
rs73580457	6:142,721,405	A/G	—	benign
rs375441704	6:142,721,616	A/G	—	likely benign
rs199876211	6:142,721,636	A/G	—	likely benign
rs1228908515	6:142,721,673	A/G	—	uncertain significance
rs758081876	6:142,721,686	C/T	—	likely benign
rs747603208	6:142,721,720	G/A	—	uncertain significance
rs373346856	6:142,721,726	C/T	—	uncertain significance
rs2223616	6:142,723,002	G/A	—	benign
rs746431638	6:142,723,144	A/G	—	uncertain significance
rs2483403625	6:142,723,150	C/T	—	uncertain significance
rs191332808	6:142,723,175	T/C	—	uncertain significance
rs9496368	6:142,723,715	T/G	—	benign
rs373975613	6:142,723,781	A/G	—	uncertain significance
rs193295605	6:142,723,795	A/G	—	uncertain significance
rs146727650	6:142,723,802	A/T	—	likely benign
rs73580458	6:142,723,851	C/T	—	likely benign
rs2483411371	6:142,723,912	A/G	—	uncertain significance
rs2483411455	6:142,723,919	C/G	—	uncertain significance
rs775155415	6:142,723,944	T/C	—	likely benign

Showing 100 of 169 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.