Oxides lacking a centre of symmetry, are highly desired as they usually bring in fascinating physical properties. However, there are limited numbers of non-centrosymmetric media in nature and most of them do not have multiple functionalities integrated. Here, using the bulk photovoltaic effect as the probing technique, we demonstrate that at interfaces with a wide range of oxides strontium titanate (SrTiO3) is polar, i.e., with broken inversion symmetry in the quantum paraelectric phase. Studies comprising conductivity and bulk photovoltaic effect on LaAlO3/SrTiO3 thin films further show excessive electronic band bending screens the induced polarity, revealing that an appropriate band bending at the interface is the key parameter to control the symmetry breaking. Inheriting the high carrier mobility from SrTiO3, the polar interface under illumination at low temperatures is conductive or metallic, permitting the multifunctionality coupling between the oxides and SrTiO3. Our studies show that significant photovoltaic effects can be generated at the polar interfaces especially in the quantum-paraelectric phase of SrTiO3, giving thus practical design strategies for multifunctional devices.