PYROXD2
pyridine nucleotide-disulphide oxidoreductase domain 2
Summary
Predicted to enable oxidoreductase activity. Involved in mitochondrion organization. Located in mitochondrial matrix. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants73 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs7905265 | 10:100,143,193 | C/G | regulatory region variant | — |
| rs1842663357 | 10:100,143,575 | T/C | — | uncertain significance |
| rs777564252 | 10:100,144,763 | T/C | — | uncertain significance |
| rs745926995 | 10:100,144,772 | A/G | — | uncertain significance |
| rs144381490 | 10:100,144,804 | C/T | — | uncertain significance |
| rs202218927 | 10:100,144,805 | A/G | — | uncertain significance |
| rs41290472 | 10:100,144,809 | C/T | — | uncertain significance |
| rs73331767 | 10:100,145,066 | G/A | intron variant | — |
| rs10883083 | 10:100,145,913 | A/T | — | — |
| rs11598867 | 10:100,146,084 | G/C | — | — |
| rs59667296 | 10:100,146,313 | A/T | intron variant | — |
| rs565590908 | 10:100,147,007 | T/C | — | uncertain significance |
| rs767160845 | 10:100,147,013 | C/T | — | uncertain significance |
| rs2496290449 | 10:100,147,025 | T/A | — | uncertain significance |
| rs1247471618 | 10:100,147,026 | C/G | — | uncertain significance |
| rs4345897 | 10:100,147,060 | A/G | synonymous variant | — |
| rs4539242 | 10:100,148,058 | T/C | regulatory region variant | — |
| rs764112886 | 10:100,148,133 | C/A | — | uncertain significance |
| rs1360568633 | 10:100,148,174 | G/C | — | uncertain significance |
| rs2147896 | 10:100,148,176 | A/C | missense variant | — |
| rs768726700 | 10:100,148,198 | C/T | — | likely benign |
| rs745550102 | 10:100,148,263 | G/C | — | uncertain significance |
| rs2147895 | 10:100,148,308 | T/G | regulatory region variant | — |
| rs2182168 | 10:100,148,353 | C/A | — | — |
| rs1013524109 | 10:100,150,368 | G/C | — | uncertain significance |
| rs2496338039 | 10:100,150,397 | T/G | — | uncertain significance |
| rs1223216822 | 10:100,150,398 | G/A | — | uncertain significance |
| rs759786016 | 10:100,150,413 | C/T | — | uncertain significance |
| rs1335953882 | 10:100,150,442 | T/C | — | uncertain significance |
| rs544916988 | 10:100,150,481 | G/A | — | uncertain significance |
| rs1397920225 | 10:100,150,494 | G/A | — | uncertain significance |
| rs774959803 | 10:100,150,791 | G/A | — | uncertain significance |
| rs10883084 | 10:100,151,189 | T/C | downstream gene variant | — |
| rs10786415 | 10:100,151,266 | A/G | downstream gene variant | — |
| rs942814 | 10:100,151,305 | A/T | — | — |
| rs6584191 | 10:100,152,055 | C/A | — | — |
| rs199640378 | 10:100,152,187 | A/C | — | uncertain significance |
| rs138250531 | 10:100,152,196 | G/A | — | uncertain significance |
| rs751689231 | 10:100,152,229 | T/C | — | uncertain significance |
| rs778010316 | 10:100,152,287 | C/G | — | uncertain significance |
| rs149406474 | 10:100,152,715 | C/A | — | uncertain significance |
| rs2496374030 | 10:100,152,719 | C/A | — | uncertain significance |
| rs139454799 | 10:100,152,748 | G/A | — | uncertain significance |
| rs145164432 | 10:100,152,788 | A/G | — | uncertain significance |
| rs1418329043 | 10:100,152,824 | G/A | — | uncertain significance |
| rs1296371348 | 10:100,154,956 | C/A | — | uncertain significance |
| rs2496412001 | 10:100,155,018 | T/G | — | uncertain significance |
| rs754819997 | 10:100,155,022 | G/A | — | uncertain significance |
| rs1429787268 | 10:100,155,024 | C/A | — | uncertain significance |
| rs1329339589 | 10:100,155,204 | T/C | — | uncertain significance |
| rs11189591 | 10:100,155,296 | T/G | upstream gene variant | — |
| rs7072216 | 10:100,156,853 | T/A | — | — |
| rs568245398 | 10:100,157,191 | G/A | — | likely benign |
| rs4488133 | 10:100,159,136 | A/G | — | — |
| rs765344749 | 10:100,159,861 | G/C | — | uncertain significance |
| rs2496479024 | 10:100,159,890 | T/G | — | uncertain significance |
| rs750974604 | 10:100,159,969 | G/C | — | uncertain significance |
| rs201923830 | 10:100,159,971 | G/C | — | uncertain significance |
| rs186622063 | 10:100,160,010 | T/C | — | uncertain significance |
| rs6584195 | 10:100,160,747 | G/A | — | — |
| rs7901577 | 10:100,164,442 | A/G | regulatory region variant | — |
| rs17455577 | 10:100,165,997 | C/T | intron variant | — |
| rs767134166 | 10:100,167,364 | T/G | — | uncertain significance |
| rs2496563225 | 10:100,167,371 | T/A | — | uncertain significance |
| rs1328778646 | 10:100,167,676 | C/T | — | uncertain significance |
| rs772866057 | 10:100,167,690 | C/T | — | uncertain significance |
| rs148396865 | 10:100,167,741 | T/G | — | uncertain significance |
| rs6584202 | 10:100,170,383 | G/C | — | — |
| rs755430794 | 10:100,170,707 | C/T | — | uncertain significance |
| rs779796674 | 10:100,174,769 | C/G | — | uncertain significance |
| rs151066099 | 10:100,174,781 | C/T | — | uncertain significance |
| rs753120165 | 10:100,174,828 | C/T | — | uncertain significance |
| rs752138434 | 10:100,174,879 | C/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.