SLC17A1
solute carrier family 17 member 1
Summary
Predicted to enable transmembrane transporter activity. Involved in sodium-dependent phosphate transport; urate metabolic process; and urate transport. Located in apical plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants91 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs182973068 | 6:25,727,801 | G/C | downstream gene variant | — |
| rs35670731 | 6:25,728,235 | C/T | downstream gene variant | — |
| rs3923725 | 6:25,734,920 | C/A | upstream gene variant | — |
| rs567942228 | 6:25,736,978 | A/G | — | — |
| rs75616507 | 6:25,761,219 | T/C | intron variant | — |
| rs3799340 | 6:25,762,646 | C/T | intron variant | — |
| rs1317817 | 6:25,765,377 | G/C | — | — |
| rs186485000 | 6:25,767,048 | A/G | intron variant | — |
| rs2275904 | 6:25,768,085 | T/A | — | — |
| rs559678870 | 6:25,769,676 | C/A | — | — |
| rs4712972 | 6:25,772,047 | A/T | — | — |
| rs1892252 | 6:25,772,639 | G/T | — | — |
| rs28412066 | 6:25,775,570 | T/G | — | — |
| rs11754288 | 6:25,776,949 | G/A | missense variant | benign |
| rs9348696 | 6:25,781,938 | A/G | downstream gene variant | — |
| rs9467596 | 6:25,783,022 | T/A | — | — |
| rs3923 | 6:25,783,315 | T/G | — | — |
| rs3757131 | 6:25,783,909 | C/T | downstream gene variant | — |
| rs35720558 | 6:25,784,800 | A/G | — | — |
| rs13197601 | 6:25,785,935 | G/A | downstream gene variant | — |
| rs13197514 | 6:25,785,991 | C/T | downstream gene variant | — |
| rs13213957 | 6:25,786,226 | T/C | downstream gene variant | — |
| rs3799344 | 6:25,786,993 | C/T | intron variant | — |
| rs2096386 | 6:25,787,817 | G/A | intron variant | — |
| rs1179086 | 6:25,791,745 | A/T | intron variant | — |
| rs942377 | 6:25,792,292 | T/C | intron variant | — |
| rs78714229 | 6:25,793,055 | T/C | intron variant | — |
| rs2762353 | 6:25,794,431 | A/C | — | — |
| rs1165216 | 6:25,797,971 | G/C | — | — |
| rs1165215 | 6:25,798,932 | G/A | intron variant | — |
| rs74521692 | 6:25,799,043 | C/T | — | benign |
| rs757891899 | 6:25,799,135 | C/T | — | uncertain significance |
| rs1763668418 | 6:25,799,137 | G/C | — | uncertain significance |
| rs1165211 | 6:25,800,922 | T/C | intron variant | — |
| rs762365919 | 6:25,801,143 | G/A | — | uncertain significance |
| rs1165209 | 6:25,801,319 | G/T | — | — |
| rs2328895 | 6:25,802,083 | C/T | intron variant | — |
| rs9467603 | 6:25,803,712 | A/G | intron variant | — |
| rs9467604 | 6:25,805,002 | A/T | intron variant | — |
| rs1177442 | 6:25,809,069 | A/G | intron variant | — |
| rs1165199 | 6:25,809,087 | C/T | intron variant | — |
| rs370460268 | 6:25,811,689 | G/A | — | likely benign |
| rs1353728715 | 6:25,811,727 | A/T | — | uncertain significance |
| rs765169684 | 6:25,811,869 | C/T | — | uncertain significance |
| rs1262375915 | 6:25,811,926 | A/T | — | uncertain significance |
| rs199533219 | 6:25,811,932 | A/G | — | uncertain significance |
| rs144074233 | 6:25,813,138 | G/A | — | uncertain significance |
| rs1165196 | 6:25,813,150 | G/A | missense variant | — |
| rs1165195 | 6:25,815,080 | T/G | intron variant | — |
| rs56031214 | 6:25,815,213 | A/T | — | — |
| rs75110987 | 6:25,815,218 | A/T | — | — |
| rs1165154 | 6:25,817,216 | T/C | intron variant | — |
| rs1165153 | 6:25,817,789 | A/T | — | — |
| rs1185567 | 6:25,818,588 | A/T | — | — |
| rs1183200 | 6:25,818,646 | G/T | — | — |
| rs2481078596 | 6:25,819,311 | C/T | — | uncertain significance |
| rs146175657 | 6:25,819,768 | C/T | — | uncertain significance |
| rs139128715 | 6:25,819,771 | T/A | — | uncertain significance |
| rs2481081503 | 6:25,819,825 | C/G | — | uncertain significance |
| rs766235950 | 6:25,820,035 | A/G | — | uncertain significance |
| rs746220690 | 6:25,820,095 | A/G | — | uncertain significance |
| rs1764492352 | 6:25,820,130 | T/A | — | uncertain significance |
| rs946466179 | 6:25,820,137 | T/C | — | likely benign |
| rs770968165 | 6:25,820,139 | G/C | — | uncertain significance |
| rs17270561 | 6:25,820,439 | C/A | intron variant | — |
| rs1165151 | 6:25,821,616 | T/G | intron variant | — |
| rs17342717 | 6:25,821,770 | C/T | intron variant | — |
| rs1747522 | 6:25,821,807 | T/C | — | — |
| rs186405009 | 6:25,823,277 | G/A | intron variant | — |
| rs1183201 | 6:25,823,444 | A/C | — | — |
| rs9467618 | 6:25,824,809 | C/T | intron variant | — |
| rs1165181 | 6:25,825,390 | T/A | intron variant | — |
| rs1165179 | 6:25,826,514 | C/T | intron variant | — |
| rs775327214 | 6:25,826,692 | T/C | — | uncertain significance |
| rs370431727 | 6:25,826,699 | T/C | — | uncertain significance |
| rs145586828 | 6:25,826,754 | C/T | — | uncertain significance |
| rs147069707 | 6:25,826,783 | G/A | — | likely benign |
| rs371028977 | 6:25,826,786 | C/T | — | uncertain significance |
| rs370150787 | 6:25,826,831 | A/C | — | uncertain significance |
| rs1408268 | 6:25,826,986 | T/A | intron variant | — |
| rs62394271 | 6:25,827,154 | T/A | intron variant | — |
| rs35875210 | 6:25,827,484 | A/G | intron variant | — |
| rs1165178 | 6:25,827,516 | A/G | intron variant | — |
| rs80176492 | 6:25,828,106 | G/A | intron variant | — |
| rs765285 | 6:25,828,242 | G/A | — | — |
| rs9467619 | 6:25,828,828 | G/C | — | — |
| rs3799354 | 6:25,830,038 | C/A | downstream gene variant | — |
| rs1165176 | 6:25,830,298 | A/C | — | — |
| rs142325882 | 6:25,830,769 | C/T | — | likely benign |
| rs3757132 | 6:25,832,691 | C/G | — | — |
| rs62394273 | 6:25,833,722 | C/T | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.