GPRIN3
GPRIN family member 3
Summary
Predicted to be involved in neuron projection development. Predicted to act upstream of or within several processes, including excitatory chemical synaptic transmission; neuronal action potential; and vitamin D receptor signaling pathway. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants48 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs34115916 | 4:90,160,486 | C/A | — | — |
| rs145667508 | 4:90,168,959 | C/G | — | uncertain significance |
| rs776817941 | 4:90,168,963 | C/T | — | uncertain significance |
| rs762749304 | 4:90,168,975 | G/A | — | uncertain significance |
| rs201266481 | 4:90,169,041 | A/C | — | uncertain significance |
| rs775390744 | 4:90,169,050 | C/T | — | uncertain significance |
| rs767364379 | 4:90,169,067 | C/T | — | uncertain significance |
| rs766826536 | 4:90,169,077 | T/C | — | likely benign |
| rs202023170 | 4:90,169,155 | C/T | — | uncertain significance |
| rs760047196 | 4:90,169,158 | C/T | — | uncertain significance |
| rs754056692 | 4:90,169,224 | G/A | — | uncertain significance |
| rs140505056 | 4:90,169,257 | C/T | — | uncertain significance |
| rs1443534638 | 4:90,169,317 | C/T | — | uncertain significance |
| rs1277960037 | 4:90,169,344 | C/T | — | uncertain significance |
| rs1204398315 | 4:90,169,388 | G/C | — | uncertain significance |
| rs148884438 | 4:90,169,424 | C/T | — | uncertain significance |
| rs1229943927 | 4:90,169,646 | T/C | — | uncertain significance |
| rs756954687 | 4:90,169,647 | T/G | — | uncertain significance |
| rs2476140511 | 4:90,169,662 | C/T | — | uncertain significance |
| rs374437786 | 4:90,169,766 | G/A | — | uncertain significance |
| rs201250233 | 4:90,169,812 | C/T | — | uncertain significance |
| rs1283016168 | 4:90,169,895 | G/T | — | uncertain significance |
| rs138037710 | 4:90,169,921 | C/A | — | uncertain significance |
| rs1275732766 | 4:90,169,968 | G/T | — | uncertain significance |
| rs375829856 | 4:90,169,969 | C/A | — | uncertain significance |
| rs761653957 | 4:90,169,977 | T/C | — | uncertain significance |
| rs551630860 | 4:90,170,027 | C/A | — | uncertain significance |
| rs560428765 | 4:90,170,045 | C/G | — | uncertain significance |
| rs752040251 | 4:90,170,070 | C/T | — | uncertain significance |
| rs144396875 | 4:90,170,170 | G/T | — | uncertain significance |
| rs770745079 | 4:90,170,220 | G/A | — | uncertain significance |
| rs28647517 | 4:90,170,237 | G/T | — | benign |
| rs999299966 | 4:90,170,369 | G/C | — | uncertain significance |
| rs1224040637 | 4:90,170,408 | G/A | — | likely benign |
| rs1184773915 | 4:90,170,429 | G/A | — | uncertain significance |
| rs151008108 | 4:90,170,442 | G/T | — | uncertain significance |
| rs570754033 | 4:90,170,582 | A/T | — | uncertain significance |
| rs1723248282 | 4:90,170,616 | C/G | — | uncertain significance |
| rs897794444 | 4:90,170,642 | C/T | — | uncertain significance |
| rs201125496 | 4:90,170,669 | G/A | — | uncertain significance |
| rs555766099 | 4:90,170,777 | G/A | — | uncertain significance |
| rs138466419 | 4:90,170,817 | A/T | — | uncertain significance |
| rs758718983 | 4:90,170,835 | G/A | — | uncertain significance |
| rs767842834 | 4:90,170,946 | T/C | — | uncertain significance |
| rs140115863 | 4:90,170,951 | C/G | — | uncertain significance |
| rs374915725 | 4:90,170,973 | G/A | — | uncertain significance |
| rs34208408 | 4:90,171,060 | C/T | — | uncertain significance |
| rs1431545 | 4:90,220,659 | C/A | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.