INSRR

insulin receptor related receptor

Summary

Enables transmembrane receptor protein tyrosine kinase activity. Involved in actin cytoskeleton organization; cellular response to alkaline pH; and protein autophosphorylation. Part of receptor complex. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants114 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs536346142	1:156,810,679	C/A	—	uncertain significance
rs1392450730	1:156,810,702	C/T	—	likely benign
rs554910069	1:156,810,754	G/A	—	uncertain significance
rs370144321	1:156,810,770	C/T	—	likely benign
rs759533268	1:156,810,808	G/A	—	uncertain significance
rs772255621	1:156,810,811	G/T	—	uncertain significance
rs754153291	1:156,810,823	T/A	—	uncertain significance
rs779655008	1:156,810,840	G/A	—	uncertain significance
rs373122172	1:156,810,901	T/C	—	benign
rs748727844	1:156,811,223	C/T	—	uncertain significance
rs1002185894	1:156,811,247	C/A	—	uncertain significance
rs778144377	1:156,811,310	C/T	—	uncertain significance
rs55694053	1:156,811,471	G/A	—	likely benign
rs754005399	1:156,811,500	C/T	—	uncertain significance
rs111433413	1:156,811,504	G/A	—	likely benign
rs139192917	1:156,811,514	C/A	—	uncertain significance
rs748854792	1:156,811,876	G/A	—	likely benign
rs147703846	1:156,811,909	A/T	—	uncertain significance
rs2525491015	1:156,811,962	G/A	—	likely benign
rs1456982232	1:156,812,015	C/T	—	uncertain significance
rs150557473	1:156,812,036	A/G	—	likely benign
rs758351138	1:156,812,058	G/T	—	uncertain significance
rs201432218	1:156,812,237	G/A	—	uncertain significance
rs767367173	1:156,812,239	G/T	—	uncertain significance
rs747115360	1:156,812,269	T/C	—	uncertain significance
rs2525494004	1:156,812,834	C/T	—	uncertain significance
rs56266370	1:156,812,880	C/T	—	likely benign
rs776355999	1:156,812,894	C/T	—	uncertain significance
rs2525494463	1:156,812,965	C/T	—	uncertain significance
rs190741064	1:156,812,975	G/A	—	uncertain significance
rs369180208	1:156,813,017	G/T	—	uncertain significance
rs763193926	1:156,813,228	C/T	—	uncertain significance
rs2525495660	1:156,813,239	T/C	—	uncertain significance
rs181833353	1:156,813,255	C/T	—	likely benign
rs775750741	1:156,814,014	C/T	—	likely benign
rs575113619	1:156,814,061	C/T	—	uncertain significance
rs148981168	1:156,814,282	G/C	—	uncertain significance
rs762614947	1:156,814,291	A/C	—	likely benign
rs369340625	1:156,814,323	C/T	—	uncertain significance
rs765450452	1:156,814,332	A/C	—	uncertain significance
rs199807142	1:156,814,548	G/A	—	uncertain significance
rs2102857146	1:156,814,558	G/T	—	uncertain significance
rs761731236	1:156,814,569	C/A	—	uncertain significance
rs1367479652	1:156,814,570	G/A	—	uncertain significance
rs1273418247	1:156,814,596	G/A	—	uncertain significance
rs1279626975	1:156,814,605	G/A	—	uncertain significance
rs761205184	1:156,814,619	A/T	—	likely benign
rs1371565436	1:156,814,882	C/A	—	uncertain significance
rs147209481	1:156,814,943	G/T	—	uncertain significance
rs56127838	1:156,815,016	C/T	—	benign
rs141332542	1:156,815,055	G/A	—	likely benign
rs778805206	1:156,815,081	C/T	—	uncertain significance
rs746321316	1:156,815,412	T/G	—	uncertain significance
rs758968003	1:156,815,414	G/A	—	uncertain significance
rs138128025	1:156,815,499	C/T	—	uncertain significance
rs751860063	1:156,815,523	A/G	—	uncertain significance
rs2525506203	1:156,815,606	C/T	—	uncertain significance
rs2525507006	1:156,815,774	C/A	—	uncertain significance
rs202160611	1:156,815,777	C/T	—	likely benign
rs376284825	1:156,815,831	G/T	—	uncertain significance
rs780030769	1:156,815,839	G/C	—	uncertain significance
rs189068345	1:156,815,916	G/A	—	benign
rs762613259	1:156,816,325	C/T	—	uncertain significance
rs138923152	1:156,816,335	C/T	—	likely benign
rs537871557	1:156,816,336	G/A	—	likely benign
rs377121387	1:156,816,385	G/C	—	uncertain significance
rs1432935301	1:156,819,092	C/G	—	uncertain significance
rs201179362	1:156,819,094	C/A	—	uncertain significance
rs140808257	1:156,819,201	G/C	—	benign
rs373665204	1:156,821,095	C/T	—	uncertain significance
rs141373320	1:156,821,096	G/A	—	likely benign
rs747408339	1:156,821,170	A/G	—	uncertain significance
rs140072588	1:156,821,198	G/A	—	benign
rs761704588	1:156,821,479	G/A	—	uncertain significance
rs368034056	1:156,821,502	C/T	—	likely benign
rs1277668841	1:156,821,516	C/T	—	uncertain significance
rs151105059	1:156,821,530	C/A	—	uncertain significance
rs768442846	1:156,821,561	C/T	—	uncertain significance
rs889486094	1:156,821,704	G/C	—	uncertain significance
rs762366667	1:156,821,716	G/T	—	uncertain significance
rs55881234	1:156,821,742	G/A	—	likely benign
rs749246577	1:156,821,762	G/C	—	uncertain significance
rs150841787	1:156,821,786	G/A	—	likely benign
rs201429290	1:156,821,803	C/T	—	uncertain significance
rs138142163	1:156,821,832	C/T	—	likely benign
rs148794008	1:156,821,846	G/A	—	likely benign
rs369907571	1:156,821,873	G/A	—	uncertain significance
rs753406751	1:156,821,915	C/T	—	uncertain significance
rs1655313516	1:156,823,585	T/C	—	uncertain significance
rs2525534040	1:156,823,597	G/T	—	uncertain significance
rs781541297	1:156,823,634	C/T	—	uncertain significance
rs148111938	1:156,823,646	C/T	—	uncertain significance
rs201403715	1:156,823,647	G/A	—	likely benign
rs963891911	1:156,823,657	T/C	—	uncertain significance
rs1345822909	1:156,823,723	A/G	—	uncertain significance
rs777435516	1:156,823,751	T/C	—	uncertain significance
rs373077572	1:156,823,774	C/T	—	uncertain significance
rs554938935	1:156,823,775	G/A	—	uncertain significance
rs55757706	1:156,823,801	G/T	—	likely benign
rs140557452	1:156,823,805	C/T	—	uncertain significance

Showing 100 of 114 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.