SLC12A7
solute carrier family 12 member 7
Summary
Enables protein kinase binding activity. Predicted to be involved in several processes, including chloride ion homeostasis; monoatomic ion transmembrane transport; and potassium ion homeostasis. Part of protein-containing complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants169 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs55861694 | 5:1,051,757 | A/C | regulatory region variant | — |
| rs3810854 | 5:1,052,360 | C/T | — | benign |
| rs374065045 | 5:1,052,488 | G/A | — | uncertain significance |
| rs2241601 | 5:1,053,216 | G/C | — | benign |
| rs2241602 | 5:1,053,341 | A/G | — | benign |
| rs2241603 | 5:1,053,396 | C/G | — | benign |
| rs914897225 | 5:1,053,538 | T/C | — | likely benign |
| rs376924487 | 5:1,053,584 | C/T | — | uncertain significance |
| rs148589244 | 5:1,053,585 | G/T | — | uncertain significance |
| rs80090801 | 5:1,053,752 | A/G | — | benign |
| rs145548600 | 5:1,056,166 | A/C | regulatory region variant | — |
| rs2241605 | 5:1,057,405 | G/A | — | benign |
| rs2241606 | 5:1,057,615 | G/A | — | benign |
| rs760266513 | 5:1,057,625 | G/A | — | uncertain significance |
| rs2531998495 | 5:1,057,638 | T/C | — | uncertain significance |
| rs527768647 | 5:1,057,724 | G/A | — | uncertain significance |
| rs12108965 | 5:1,057,782 | T/C | — | benign |
| rs2241607 | 5:1,057,890 | G/A | — | benign |
| rs35791340 | 5:1,057,960 | T/C | — | benign |
| rs111552633 | 5:1,058,036 | G/A | downstream gene variant | — |
| rs62329239 | 5:1,058,119 | G/C | — | — |
| rs4975699 | 5:1,060,366 | G/C | — | benign |
| rs35661060 | 5:1,060,379 | G/A | — | benign |
| rs4975568 | 5:1,060,400 | G/A | — | benign |
| rs143654475 | 5:1,060,463 | C/T | — | uncertain significance |
| rs201904847 | 5:1,060,520 | A/G | — | uncertain significance |
| rs776669983 | 5:1,060,538 | T/C | — | uncertain significance |
| rs4246750 | 5:1,060,634 | C/T | — | benign |
| rs4246749 | 5:1,060,654 | G/A | — | benign |
| rs2241608 | 5:1,060,685 | G/A | — | benign |
| rs11133609 | 5:1,060,795 | G/A | — | benign |
| rs4246748 | 5:1,060,804 | C/T | — | benign |
| rs4975567 | 5:1,060,831 | G/A | — | benign |
| rs184475122 | 5:1,063,779 | G/A | upstream gene variant | — |
| rs1561040378 | 5:1,063,961 | T/A | — | uncertain significance |
| rs765374153 | 5:1,063,979 | C/T | — | uncertain significance |
| rs752308479 | 5:1,063,995 | G/C | — | uncertain significance |
| rs7722287 | 5:1,063,998 | A/G | — | benign |
| rs2532057601 | 5:1,064,029 | T/C | — | uncertain significance |
| rs762100587 | 5:1,064,042 | C/G | — | uncertain significance |
| rs55792623 | 5:1,064,100 | G/A | — | likely benign |
| rs138300444 | 5:1,064,208 | C/T | — | uncertain significance |
| rs574433513 | 5:1,064,209 | G/A | — | uncertain significance |
| rs1372556823 | 5:1,064,245 | C/T | — | uncertain significance |
| rs143746308 | 5:1,064,264 | G/A | — | benign |
| rs758516630 | 5:1,064,281 | C/G | — | uncertain significance |
| rs201925892 | 5:1,064,307 | G/A | — | likely benign |
| rs200262061 | 5:1,064,311 | C/T | — | uncertain significance |
| rs375034450 | 5:1,064,339 | G/C | — | likely benign |
| rs375569381 | 5:1,064,347 | C/T | — | likely benign |
| rs4362981 | 5:1,065,290 | A/G | — | benign |
| rs62331176 | 5:1,065,297 | C/T | — | benign |
| rs79273934 | 5:1,065,301 | G/A | — | benign |
| rs737154 | 5:1,065,399 | C/T | — | benign |
| rs373925941 | 5:1,065,415 | G/A | — | uncertain significance |
| rs746519418 | 5:1,065,431 | C/T | — | uncertain significance |
| rs56078134 | 5:1,065,683 | A/C | — | benign |
| rs13186367 | 5:1,065,689 | C/T | — | benign |
| rs10780095 | 5:1,073,689 | C/T | — | benign |
| rs199974381 | 5:1,073,756 | C/A | — | uncertain significance |
| rs148462588 | 5:1,073,758 | C/T | — | likely benign |
| rs200905878 | 5:1,073,759 | G/A | — | uncertain significance |
| rs146019944 | 5:1,073,803 | G/A | — | likely benign |
| rs754679636 | 5:1,073,810 | C/T | — | uncertain significance |
| rs371278849 | 5:1,073,842 | G/A | — | uncertain significance |
| rs150018091 | 5:1,073,861 | G/A | — | uncertain significance |
| rs149182820 | 5:1,073,883 | C/T | — | benign |
| rs145211606 | 5:1,073,886 | G/A | — | benign |
| rs6895800 | 5:1,074,360 | A/G | — | benign |
| rs12523242 | 5:1,074,560 | C/A | — | benign |
| rs369556020 | 5:1,074,718 | C/T | — | uncertain significance |
| rs372314314 | 5:1,074,719 | G/A | — | uncertain significance |
| rs41280366 | 5:1,074,818 | T/C | — | benign |
| rs7714914 | 5:1,074,921 | G/A | — | benign |
| rs11133613 | 5:1,075,051 | G/A | — | benign |
| rs150315797 | 5:1,075,488 | G/A | — | benign |
| rs771075055 | 5:1,075,489 | C/T | — | uncertain significance |
| rs6866735 | 5:1,076,129 | T/C | — | benign |
| rs11951420 | 5:1,076,245 | A/G | — | benign |
| rs570062685 | 5:1,076,292 | C/T | — | uncertain significance |
| rs11952124 | 5:1,076,459 | T/G | — | benign |
| rs74673540 | 5:1,076,706 | C/T | — | benign |
| rs372638882 | 5:1,076,903 | C/T | — | uncertain significance |
| rs1400999392 | 5:1,076,911 | T/C | — | uncertain significance |
| rs13156064 | 5:1,077,680 | T/C | — | benign |
| rs55973529 | 5:1,077,822 | A/C | — | benign |
| rs748183336 | 5:1,077,962 | C/T | — | likely benign |
| rs148501261 | 5:1,077,973 | C/T | — | benign |
| rs751886456 | 5:1,077,997 | G/A | — | uncertain significance |
| rs757403501 | 5:1,078,067 | G/A | — | uncertain significance |
| rs751647758 | 5:1,078,088 | C/T | — | uncertain significance |
| rs1738563020 | 5:1,078,093 | A/G | — | uncertain significance |
| rs4975684 | 5:1,078,642 | C/A | — | benign |
| rs151053159 | 5:1,078,832 | C/T | missense variant | — |
| rs4975564 | 5:1,078,898 | G/A | — | benign |
| rs79172727 | 5:1,079,070 | T/G | — | benign |
| rs745481788 | 5:1,079,516 | T/C | — | uncertain significance |
| rs774595734 | 5:1,079,550 | C/T | — | likely benign |
| rs752930961 | 5:1,079,582 | C/T | — | uncertain significance |
| rs13176210 | 5:1,081,668 | G/A | — | benign |
Showing 100 of 169 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.