GREB1L

GREB1 like retinoic acid receptor coactivator

Summary

Acts upstream of or within kidney development. Predicted to be located in membrane. Implicated in autosomal dominant nonsyndromic deafness 80 and renal agenesis. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants284 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs1268367147	18:18,834,032	T/G	—	—
rs73432789	18:18,963,473	G/A	—	benign
rs1292048024	18:18,963,493	A/G	—	uncertain significance
rs2144055899	18:18,963,499	G/A	—	uncertain significance
rs1212136611	18:18,963,502	A/C	—	likely pathogenic
rs777707946	18:18,963,516	C/T	—	likely pathogenic
rs2510788281	18:18,963,553	C/T	—	uncertain significance
rs895725133	18:18,963,571	T/G	—	uncertain significance
rs532181089	18:18,963,573	G/A	—	likely benign
rs1041617291	18:18,963,576	C/G	—	likely benign
rs1567966432	18:18,963,590	T/G	—	likely pathogenic
rs2510789361	18:18,963,636	G/A	—	uncertain significance
rs561720231	18:18,964,151	T/C	—	likely benign
rs747354969	18:18,964,168	T/C	—	likely benign
rs753311521	18:18,964,175	C/A	—	uncertain significance
rs370589003	18:18,964,212	G/A	—	uncertain significance
rs2510796455	18:18,964,235	G/A	—	uncertain significance
rs185578147	18:18,964,286	G/A	—	conflicting classifications of pathogenicity
rs772804626	18:18,964,306	C/T	—	likely benign
rs1254264958	18:18,964,320	C/T	—	likely pathogenic
rs1333304296	18:18,964,356	C/T	—	uncertain significance
rs1479687090	18:18,975,364	A/G	—	uncertain significance
rs1598751507	18:18,975,373	G/A	—	association
rs555628599	18:18,975,380	A/G	—	likely benign
rs2041014360	18:18,975,399	A/C	—	uncertain significance
rs371012004	18:18,975,445	A/G	—	uncertain significance
rs757376952	18:18,975,500	T/A	—	likely benign
rs2510905016	18:18,975,527	G/A	—	uncertain significance
rs16941439	18:18,975,534	A/G	—	benign
rs1187506481	18:18,981,094	G/A	—	likely benign
rs2144520227	18:18,981,131	G/A	—	uncertain significance
rs2510947992	18:18,981,144	G/A	—	uncertain significance
rs1274267669	18:18,981,153	G/A	—	uncertain significance
rs2041304305	18:18,981,223	A/G	—	likely benign
rs2510948451	18:18,981,261	C/T	—	uncertain significance
rs2144522176	18:18,981,283	G/T	—	pathogenic
rs147048716	18:18,983,845	G/A	—	likely benign
rs551864882	18:18,983,906	C/T	—	likely benign
rs1598769185	18:18,983,941	G/T	—	association
rs4800660	18:18,991,874	T/C	intron variant	—
rs118035855	18:18,994,683	G/A	intron variant	—
rs1363959539	18:19,019,477	T/C	—	likely benign
rs2511343375	18:19,019,482	A/T	—	uncertain significance
rs2033773650	18:19,019,497	A/G	—	likely pathogenic
rs2511343875	18:19,019,524	C/T	—	uncertain significance
rs2511344279	18:19,019,550	G/C	—	uncertain significance
rs2511344570	18:19,019,569	C/T	—	uncertain significance
rs1407912822	18:19,020,242	T/A	—	uncertain significance
rs1287687444	18:19,020,248	G/A	—	uncertain significance
rs2033826794	18:19,020,254	C/T	—	uncertain significance
rs1555648043	18:19,020,262	C/T	—	pathogenic
rs1311814599	18:19,020,263	G/A	—	uncertain significance
rs377314861	18:19,020,268	C/T	—	uncertain significance
rs538653254	18:19,020,342	A/G	—	likely benign
rs1041442097	18:19,020,348	G/A	—	uncertain significance
rs1036639935	18:19,021,362	G/A	—	likely benign
rs2511364275	18:19,021,394	C/G	—	uncertain significance
rs764822745	18:19,021,415	C/G	—	uncertain significance
rs116887099	18:19,021,462	C/G	—	uncertain significance
rs775822553	18:19,021,482	A/G	—	likely benign
rs754658709	18:19,024,176	T/C	—	likely benign
rs2511388966	18:19,024,242	T/C	—	uncertain significance
rs200509926	18:19,024,255	C/G	—	uncertain significance
rs2511389119	18:19,024,260	A/G	—	uncertain significance
rs1201583875	18:19,024,299	G/C	—	uncertain significance
rs371826632	18:19,024,307	G/A	—	benign
rs775869656	18:19,024,325	G/A	—	uncertain significance
rs575494010	18:19,024,347	C/T	—	likely benign
rs140882830	18:19,024,365	G/A	—	benign
rs570797238	18:19,029,465	A/G	—	benign
rs2511437248	18:19,029,503	G/A	—	uncertain significance
rs34656972	18:19,029,515	C/T	—	benign
rs2034416371	18:19,029,551	G/C	—	uncertain significance
rs1598859662	18:19,029,567	C/G	—	association
rs2511438193	18:19,029,582	T/C	—	uncertain significance
rs531502857	18:19,029,625	C/T	—	likely benign
rs747371319	18:19,029,626	G/A	—	uncertain significance
rs1474031482	18:19,029,635	G/A	—	uncertain significance
rs1372598805	18:19,029,647	G/A	—	uncertain significance
rs887917846	18:19,029,655	G/A	—	likely benign
rs2511439289	18:19,029,670	G/A	—	likely benign
rs970335044	18:19,029,705	G/A	—	uncertain significance
rs1035683785	18:19,029,731	C/T	—	uncertain significance
rs1462783728	18:19,029,739	T/C	—	likely benign
rs1422032806	18:19,029,760	G/A	—	likely benign
rs557226726	18:19,029,779	T/C	—	uncertain significance
rs1220903701	18:19,029,785	G/A	—	uncertain significance
rs2145407319	18:19,029,802	G/A	—	uncertain significance
rs192602511	18:19,030,972	T/C	—	benign
rs2511453409	18:19,030,992	C/T	—	likely pathogenic
rs2034496911	18:19,030,998	C/T	—	pathogenic
rs1555650110	18:19,031,043	G/T	—	pathogenic
rs781345673	18:19,031,073	G/A	—	uncertain significance
rs115901628	18:19,031,122	T/C	—	benign
rs1482332053	18:19,032,038	T/C	—	likely benign
rs1382939744	18:19,032,046	G/A	—	uncertain significance
rs748258684	18:19,032,095	G/C	—	uncertain significance
rs2034559099	18:19,032,130	T/C	—	uncertain significance
rs1208372191	18:19,032,169	C/T	—	pathogenic
rs2511464713	18:19,032,181	A/C	—	likely pathogenic

Showing 100 of 284 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.