HSPA12A
heat shock protein family A (Hsp70) member 12A
Summary
Predicted to enable ATP binding activity. Predicted to act upstream of or within several processes, including import into nucleus; liver development; and macrophage activation. Located in extracellular exosome. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants47 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs369963832 | 10:118,434,341 | A/G | — | uncertain significance |
| rs782412500 | 10:118,434,342 | T/C | — | uncertain significance |
| rs868970051 | 10:118,434,375 | C/T | — | uncertain significance |
| rs375255169 | 10:118,434,563 | C/T | — | uncertain significance |
| rs146839286 | 10:118,434,621 | C/T | — | uncertain significance |
| rs187495430 | 10:118,434,636 | G/A | — | uncertain significance |
| rs781946508 | 10:118,434,699 | C/T | — | uncertain significance |
| rs200715815 | 10:118,434,744 | C/T | — | uncertain significance |
| rs202107187 | 10:118,434,750 | C/A | — | uncertain significance |
| rs782470572 | 10:118,434,812 | C/T | — | uncertain significance |
| rs1033829945 | 10:118,434,858 | G/A | — | uncertain significance |
| rs782819530 | 10:118,434,864 | C/T | — | uncertain significance |
| rs782537687 | 10:118,434,909 | C/T | — | uncertain significance |
| rs782107484 | 10:118,435,929 | A/T | — | uncertain significance |
| rs575016908 | 10:118,435,951 | G/A | — | uncertain significance |
| rs782487879 | 10:118,435,952 | C/T | — | uncertain significance |
| rs1554878297 | 10:118,439,167 | G/C | — | uncertain significance |
| rs1554878304 | 10:118,439,205 | C/A | — | uncertain significance |
| rs781918083 | 10:118,439,234 | C/T | — | uncertain significance |
| rs781974587 | 10:118,440,729 | C/T | — | uncertain significance |
| rs782489411 | 10:118,440,752 | A/G | — | uncertain significance |
| rs199615590 | 10:118,441,322 | A/G | — | uncertain significance |
| rs1311274453 | 10:118,443,308 | T/A | — | uncertain significance |
| rs782609994 | 10:118,443,319 | C/G | — | uncertain significance |
| rs781929997 | 10:118,443,335 | C/T | — | likely benign |
| rs782064654 | 10:118,443,350 | C/T | — | uncertain significance |
| rs1195155414 | 10:118,443,388 | C/T | — | uncertain significance |
| rs375461005 | 10:118,443,416 | C/T | — | uncertain significance |
| rs1398154073 | 10:118,443,440 | G/C | — | uncertain significance |
| rs11197796 | 10:118,451,842 | C/T | intron variant | — |
| rs371208406 | 10:118,451,912 | C/T | — | uncertain significance |
| rs782137661 | 10:118,451,956 | G/A | — | uncertain significance |
| rs2493380218 | 10:118,451,957 | A/C | — | uncertain significance |
| rs12259842 | 10:118,455,243 | C/T | intron variant | — |
| rs140035360 | 10:118,455,797 | C/T | intron variant | — |
| rs1377333802 | 10:118,458,165 | A/C | — | uncertain significance |
| rs781817907 | 10:118,460,573 | C/T | — | uncertain significance |
| rs1554882213 | 10:118,464,685 | C/A | — | uncertain significance |
| rs1638429 | 10:118,475,976 | T/C | — | — |
| rs1665650 | 10:118,487,100 | T/C | intron variant | — |
| rs1248793492 | 10:118,501,950 | C/A | — | uncertain significance |
| rs189665125 | 10:118,525,222 | A/G | regulatory region variant | — |
| rs75572469 | 10:118,544,154 | G/A | intergenic variant | — |
| rs138802039 | 10:118,558,011 | C/A | — | — |
| rs7912336 | 10:118,558,736 | A/T | intergenic variant | — |
| rs740363 | 10:118,575,606 | G/A | regulatory region variant | — |
| rs1626678 | 10:118,576,146 | G/A | intergenic variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.