SLC10A7
solute carrier family 10 member 7
Summary
Predicted to enable symporter activity. Involved in bone development; heparin proteoglycan biosynthetic process; and intracellular calcium ion homeostasis. Located in Golgi apparatus; endoplasmic reticulum; and plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants49 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs573036097 | 4:147,178,018 | T/C | — | likely benign |
| rs1404132097 | 4:147,178,069 | C/A | — | uncertain significance |
| rs138035413 | 4:147,179,909 | C/T | — | likely benign |
| rs760016229 | 4:147,179,969 | C/T | — | uncertain significance |
| rs72727994 | 4:147,198,186 | C/T | intron variant | — |
| rs754697850 | 4:147,214,105 | A/C | — | uncertain significance |
| rs369056739 | 4:147,214,124 | T/C | — | uncertain significance |
| rs773117913 | 4:147,214,148 | T/C | — | pathogenic |
| rs76346232 | 4:147,215,092 | T/C | — | benign |
| rs148698801 | 4:147,215,100 | C/A | — | likely benign |
| rs2547180949 | 4:147,215,111 | T/A | — | uncertain significance |
| rs1169149434 | 4:147,215,126 | T/C | — | uncertain significance |
| rs373948151 | 4:147,215,130 | G/A | — | uncertain significance |
| rs759768158 | 4:147,215,170 | G/A | — | likely benign |
| rs201948152 | 4:147,215,190 | T/C | — | likely benign |
| rs568214752 | 4:147,221,848 | G/A | — | — |
| rs6854541 | 4:147,226,374 | A/G | — | — |
| rs1560782372 | 4:147,227,080 | G/A | — | pathogenic |
| rs2149681892 | 4:147,227,133 | G/A | — | uncertain significance |
| rs2547234436 | 4:147,247,123 | A/G | — | uncertain significance |
| rs147461877 | 4:147,247,142 | C/T | — | likely benign |
| rs2547234601 | 4:147,247,147 | C/T | — | uncertain significance |
| rs72729847 | 4:147,296,930 | T/C | intron variant | — |
| rs191493117 | 4:147,360,131 | C/T | intron variant | — |
| rs778642245 | 4:147,363,926 | T/C | — | likely benign |
| rs373382583 | 4:147,363,964 | T/A | — | likely benign |
| rs78029235 | 4:147,393,387 | C/T | intron variant | — |
| rs747827453 | 4:147,424,993 | T/C | — | likely benign |
| rs1560973467 | 4:147,425,009 | C/T | — | pathogenic |
| rs2547555978 | 4:147,425,053 | G/A | — | uncertain significance |
| rs1560973571 | 4:147,425,062 | C/T | — | pathogenic |
| rs7439061 | 4:147,425,114 | A/T | — | benign |
| rs2547569717 | 4:147,431,094 | G/C | — | uncertain significance |
| rs2547569779 | 4:147,431,116 | A/C | — | uncertain significance |
| rs781346106 | 4:147,431,145 | A/C | — | likely benign |
| rs1476606807 | 4:147,431,154 | C/A | — | uncertain significance |
| rs1560980659 | 4:147,431,164 | A/G | — | pathogenic |
| rs2547569935 | 4:147,431,169 | C/T | — | likely benign |
| rs1560980728 | 4:147,431,201 | C/A | — | pathogenic |
| rs139872057 | 4:147,438,211 | A/G | — | benign |
| rs775473288 | 4:147,438,213 | T/C | — | uncertain significance |
| rs1738080227 | 4:147,438,277 | A/G | — | likely benign |
| rs182882951 | 4:147,442,750 | G/A | — | benign |
| rs149837412 | 4:147,442,779 | C/A | — | uncertain significance |
| rs2530097182 | 4:147,442,781 | C/T | — | uncertain significance |
| rs776442200 | 4:147,442,787 | G/C | — | uncertain significance |
| rs1454653744 | 4:147,442,827 | C/G | — | uncertain significance |
| rs2530098554 | 4:147,442,844 | T/G | — | uncertain significance |
| rs116538438 | 4:147,442,852 | T/G | — | benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.