PPP1R26

protein phosphatase 1 regulatory subunit 26

Summary

Predicted to enable protein phosphatase inhibitor activity. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants100 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs2777324	9:138,374,898	T/C	upstream gene variant	—
rs2254812	9:138,375,872	G/A	—	—
rs139821365	9:138,376,372	G/A	—	uncertain significance
rs371967332	9:138,376,373	C/T	—	uncertain significance
rs774750336	9:138,376,438	C/A	—	uncertain significance
rs199947269	9:138,376,477	G/C	—	uncertain significance
rs367729948	9:138,376,478	C/T	—	uncertain significance
rs773741384	9:138,376,481	C/G	—	uncertain significance
rs963098862	9:138,376,495	G/T	—	uncertain significance
rs201579051	9:138,376,528	G/A	—	uncertain significance
rs142346595	9:138,376,538	G/A	—	uncertain significance
rs767484243	9:138,376,556	G/A	—	likely benign
rs142421416	9:138,376,621	G/C	—	uncertain significance
rs533250185	9:138,376,639	G/A	—	likely benign
rs1787144475	9:138,376,697	C/T	—	uncertain significance
rs757134095	9:138,376,807	G/A	—	uncertain significance
rs372323498	9:138,376,858	G/A	—	uncertain significance
rs749163916	9:138,376,928	T/G	—	uncertain significance
rs763204394	9:138,377,039	C/T	—	uncertain significance
rs754898129	9:138,377,071	C/G	—	uncertain significance
rs192421657	9:138,377,108	A/G	—	uncertain significance
rs1366384071	9:138,377,192	G/A	—	likely benign
rs141353268	9:138,377,272	A/G	—	uncertain significance
rs868766086	9:138,377,318	C/T	—	uncertain significance
rs761538566	9:138,377,333	G/A	—	uncertain significance
rs201945292	9:138,377,350	C/G	—	uncertain significance
rs199863193	9:138,377,383	G/T	—	uncertain significance
rs1213288648	9:138,377,428	G/A	—	uncertain significance
rs150815603	9:138,377,540	G/A	—	uncertain significance
rs774517402	9:138,377,570	A/G	—	uncertain significance
rs756321419	9:138,377,605	G/C	—	uncertain significance
rs773780758	9:138,377,675	G/T	—	uncertain significance
rs1300800285	9:138,377,689	C/T	—	uncertain significance
rs2490671806	9:138,377,692	G/A	—	uncertain significance
rs368798891	9:138,377,732	C/T	—	likely benign
rs147504115	9:138,377,746	A/G	—	uncertain significance
rs1371417596	9:138,377,748	G/A	—	likely benign
rs765445905	9:138,377,777	G/A	—	uncertain significance
rs1664029816	9:138,377,854	G/A	—	uncertain significance
rs1049541401	9:138,377,864	A/G	—	uncertain significance
rs369103070	9:138,377,870	C/T	—	uncertain significance
rs749490669	9:138,377,896	T/C	—	likely benign
rs146976488	9:138,377,900	C/T	—	uncertain significance
rs376063346	9:138,377,905	G/T	—	uncertain significance
rs1175368772	9:138,377,971	C/T	—	uncertain significance
rs201516502	9:138,378,035	A/C	—	likely benign
rs766014114	9:138,378,078	G/C	—	uncertain significance
rs754345072	9:138,378,080	C/A	—	uncertain significance
rs139362521	9:138,378,143	G/A	—	uncertain significance
rs539316336	9:138,378,157	C/T	—	uncertain significance
rs2490682136	9:138,378,202	G/A	—	uncertain significance
rs746861407	9:138,378,322	C/T	—	uncertain significance
rs745512822	9:138,378,462	G/T	—	uncertain significance
rs189673212	9:138,378,506	C/T	—	uncertain significance
rs2490687726	9:138,378,511	A/G	—	uncertain significance
rs767390657	9:138,378,535	G/T	—	uncertain significance
rs374959708	9:138,378,572	G/A	—	likely benign
rs1304212075	9:138,378,592	G/C	—	uncertain significance
rs755823460	9:138,378,637	A/G	—	uncertain significance
rs200773477	9:138,378,643	G/A	—	uncertain significance
rs753409498	9:138,378,644	A/G	—	uncertain significance
rs757866413	9:138,378,721	G/C	—	uncertain significance
rs147012627	9:138,378,725	C/T	—	uncertain significance
rs776560398	9:138,378,754	G/A	—	uncertain significance
rs61736979	9:138,378,772	G/A	—	uncertain significance
rs370760585	9:138,378,928	G/A	—	likely benign
rs777825980	9:138,378,959	C/T	—	uncertain significance
rs199883887	9:138,379,010	C/T	—	likely benign
rs372832870	9:138,379,018	G/A	—	likely benign
rs753775579	9:138,379,027	C/T	—	uncertain significance
rs746681258	9:138,379,038	G/T	—	uncertain significance
rs148597772	9:138,379,063	G/A	—	uncertain significance
rs769355885	9:138,379,097	A/G	—	uncertain significance
rs147761248	9:138,379,154	G/A	—	uncertain significance
rs141129802	9:138,379,159	G/T	—	uncertain significance
rs748442143	9:138,379,171	C/G	—	uncertain significance
rs143121134	9:138,379,260	G/A	—	likely benign
rs1431419403	9:138,379,340	G/T	—	uncertain significance
rs375360481	9:138,379,441	G/A	—	uncertain significance
rs762485181	9:138,379,484	G/A	—	uncertain significance
rs775313091	9:138,379,487	C/G	—	uncertain significance
rs752087422	9:138,379,489	G/A	—	uncertain significance
rs757883136	9:138,379,511	G/A	—	likely benign
rs780280278	9:138,379,516	G/T	—	uncertain significance
rs1054706140	9:138,379,523	G/A	—	uncertain significance
rs770913387	9:138,379,526	G/T	—	uncertain significance
rs570749929	9:138,379,559	G/A	—	uncertain significance
rs981110234	9:138,379,646	G/A	—	uncertain significance
rs756076952	9:138,379,664	T/C	—	uncertain significance
rs1351804744	9:138,379,678	G/C	—	uncertain significance
rs759779989	9:138,379,706	C/T	—	uncertain significance
rs2490717383	9:138,379,739	C/G	—	uncertain significance
rs778889304	9:138,379,762	C/G	—	uncertain significance
rs1442337880	9:138,379,808	C/T	—	uncertain significance
rs374451433	9:138,379,844	C/T	—	uncertain significance
rs371561109	9:138,379,882	G/A	—	uncertain significance
rs140932687	9:138,379,894	G/A	—	uncertain significance
rs762786759	9:138,379,909	G/A	—	uncertain significance
rs368262533	9:138,379,939	G/A	—	uncertain significance
rs188142301	9:138,381,085	A/G	downstream gene variant	—

Gene information from NCBI Gene. Variant classifications from ClinVar.