PPP1R37

protein phosphatase 1 regulatory subunit 37

Summary

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

Known Variants72 total

rsidPosition (GRCh37)AllelesClassClinVar
rs136889089119:45,596,618C/Tuncertain significance
rs196794859519:45,596,674G/Tuncertain significance
rs146497538719:45,596,729C/Guncertain significance
rs1246204019:45,612,226C/Tintron variant
rs3454571319:45,614,601C/Tintron variant
rs200435719:45,618,959G/Aintron variant
rs11340586919:45,620,513G/Tregulatory region variant
rs54736428919:45,623,466A/G
rs37559498719:45,623,467A/G
rs53108549019:45,623,967G/A
rs1040508619:45,627,235C/Tupstream gene variant
rs75436619:45,633,686G/Aregulatory region variant
rs2862049019:45,638,245C/A
rs7740130519:45,641,106C/A
rs92690264119:45,641,810A/Cuncertain significance
rs99274504219:45,641,819T/Auncertain significance
rs118840885819:45,641,846C/Guncertain significance
rs1040115719:45,642,044G/Aupstream gene variant
rs20144486219:45,643,509G/Auncertain significance
rs94328580319:45,643,521G/Auncertain significance
rs91187091919:45,643,779A/Guncertain significance
rs7827312519:45,644,354A/Tupstream gene variant
rs55847281419:45,644,639C/Guncertain significance
rs93872297919:45,645,347G/Auncertain significance
rs76612313619:45,645,353C/Tuncertain significance
rs135055681119:45,645,374C/Tuncertain significance
rs88708871219:45,645,388C/Tuncertain significance
rs196862070519:45,645,391G/Auncertain significance
rs134324623719:45,645,445T/Auncertain significance
rs98704098119:45,645,452G/Auncertain significance
rs75486282619:45,645,623G/Auncertain significance
rs251378129419:45,646,813G/Cuncertain significance
rs88711717319:45,646,870G/Tuncertain significance
rs53551873319:45,648,112C/Tuncertain significance
rs77871555119:45,648,154C/Guncertain significance
rs86858401119:45,648,157A/Guncertain significance
rs128173771919:45,648,200G/Auncertain significance
rs104834800519:45,648,203A/Guncertain significance
rs77340774519:45,648,411C/Tuncertain significance
rs90638461119:45,648,498C/Tuncertain significance
rs196867333819:45,648,508A/Guncertain significance
rs97263506319:45,648,625C/Guncertain significance
rs14409911319:45,648,662G/Auncertain significance
rs128690199519:45,648,701G/Cuncertain significance
rs52939627019:45,648,729C/Tuncertain significance
rs131297451319:45,648,779G/Auncertain significance
rs251378311419:45,648,800G/Auncertain significance
rs86832458719:45,648,812G/Auncertain significance
rs251378314819:45,648,821C/Guncertain significance
rs97228219019:45,648,839T/Cuncertain significance
rs75774340419:45,648,840C/Guncertain significance
rs75443201619:45,648,891C/Tuncertain significance
rs74964232319:45,648,945G/Auncertain significance
rs145386170119:45,648,954G/Auncertain significance
rs98847152819:45,648,981G/Auncertain significance
rs105023889419:45,648,999C/Guncertain significance
rs124260754919:45,649,014A/Guncertain significance
rs103796694119:45,649,034G/Cuncertain significance
rs137298934719:45,649,049G/Auncertain significance
rs124583575419:45,649,060G/Cuncertain significance
rs135577347419:45,649,077C/Tlikely benign
rs76528839819:45,649,081T/Cbenign
rs115836135919:45,649,088C/Auncertain significance
rs75656895119:45,649,112G/Tuncertain significance
rs86646324619:45,649,127C/Tuncertain significance
rs119028204219:45,649,134C/Tuncertain significance
rs77247533119:45,649,152G/Alikely benign
rs93184066419:45,649,232G/Auncertain significance
rs88804798519:45,649,259C/Tuncertain significance
rs90454365719:45,649,260C/Tuncertain significance
rs77912924119:45,649,295G/Auncertain significance
rs143523366819:45,649,651T/Cuncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.