ZNF592
zinc finger protein 592
Summary
This gene is thought to play a role in a complex developmental pathway and the regulation of genes involved in cerebellar development. Mutations in this gene have been associated with autosomal recessive spinocerebellar ataxia. [provided by RefSeq, Jan 2011]
Known Variants106 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs12903256 | 15:85,308,141 | G/T | — | — |
| rs75652600 | 15:85,311,291 | A/T | — | — |
| rs8023658 | 15:85,323,220 | G/T | — | — |
| rs145351255 | 15:85,325,991 | G/C | — | uncertain significance |
| rs372898907 | 15:85,326,024 | C/T | — | uncertain significance |
| rs145206161 | 15:85,326,075 | T/G | — | conflicting classifications of pathogenicity |
| rs758215815 | 15:85,326,088 | C/T | — | uncertain significance |
| rs144989451 | 15:85,326,089 | C/T | — | likely benign |
| rs1387827683 | 15:85,326,097 | C/T | — | uncertain significance |
| rs756436525 | 15:85,326,162 | A/G | — | uncertain significance |
| rs201486461 | 15:85,326,172 | G/A | — | uncertain significance |
| rs557600795 | 15:85,326,184 | A/G | — | uncertain significance |
| rs2505637045 | 15:85,326,198 | T/C | — | likely benign |
| rs199775065 | 15:85,326,285 | C/A | — | benign |
| rs143182143 | 15:85,326,313 | C/G | — | uncertain significance |
| rs1356706485 | 15:85,326,370 | A/G | — | uncertain significance |
| rs371305645 | 15:85,326,374 | C/T | — | likely benign |
| rs200524575 | 15:85,326,375 | G/A | — | uncertain significance |
| rs777121110 | 15:85,326,390 | C/T | — | uncertain significance |
| rs772928025 | 15:85,326,420 | C/A | — | uncertain significance |
| rs151234929 | 15:85,326,421 | C/G | — | uncertain significance |
| rs140210043 | 15:85,326,432 | G/A | — | uncertain significance |
| rs372238385 | 15:85,326,475 | C/T | — | uncertain significance |
| rs2505638187 | 15:85,326,511 | A/G | — | uncertain significance |
| rs760402025 | 15:85,326,520 | C/T | — | uncertain significance |
| rs776741627 | 15:85,326,525 | C/G | — | uncertain significance |
| rs752209667 | 15:85,326,570 | G/C | — | uncertain significance |
| rs1225296584 | 15:85,326,577 | A/G | — | uncertain significance |
| rs142431765 | 15:85,326,594 | A/C | — | uncertain significance |
| rs150122607 | 15:85,326,602 | G/A | — | likely benign |
| rs375076818 | 15:85,326,622 | G/A | — | uncertain significance |
| rs1567069544 | 15:85,326,682 | C/T | — | uncertain significance |
| rs1962485507 | 15:85,326,711 | C/G | — | uncertain significance |
| rs769657850 | 15:85,326,714 | C/G | — | uncertain significance |
| rs372605775 | 15:85,326,715 | C/T | — | uncertain significance |
| rs61736261 | 15:85,326,798 | A/G | — | benign |
| rs778157390 | 15:85,326,807 | A/C | — | uncertain significance |
| rs749011102 | 15:85,326,813 | G/C | — | uncertain significance |
| rs147251641 | 15:85,326,834 | G/T | — | uncertain significance |
| rs144705583 | 15:85,326,904 | G/A | — | uncertain significance |
| rs61737677 | 15:85,326,955 | G/A | — | benign |
| rs1962494748 | 15:85,326,983 | A/T | — | uncertain significance |
| rs958494207 | 15:85,327,164 | G/A | — | uncertain significance |
| rs1962511041 | 15:85,327,329 | C/T | — | uncertain significance |
| rs144163979 | 15:85,327,333 | G/A | — | uncertain significance |
| rs143880466 | 15:85,327,524 | C/T | — | uncertain significance |
| rs751983283 | 15:85,327,588 | G/C | — | uncertain significance |
| rs868816313 | 15:85,327,599 | G/A | — | uncertain significance |
| rs533562706 | 15:85,327,656 | G/A | — | uncertain significance |
| rs770412639 | 15:85,327,737 | G/A | — | uncertain significance |
| rs200137485 | 15:85,327,839 | G/A | — | uncertain significance |
| rs752895625 | 15:85,327,879 | C/T | — | uncertain significance |
| rs139025399 | 15:85,327,915 | C/T | — | uncertain significance |
| rs2505644488 | 15:85,327,986 | C/T | — | uncertain significance |
| rs752592509 | 15:85,328,007 | C/G | — | uncertain significance |
| rs770560208 | 15:85,328,037 | A/G | — | uncertain significance |
| rs746252249 | 15:85,328,067 | C/T | — | uncertain significance |
| rs3748376 | 15:85,328,352 | C/T | — | benign |
| rs12906348 | 15:85,329,421 | A/C | intron variant | — |
| rs2241645 | 15:85,333,953 | A/G | — | benign |
| rs201554213 | 15:85,333,957 | C/T | — | likely benign |
| rs376104089 | 15:85,334,047 | C/G | — | uncertain significance |
| rs2241644 | 15:85,334,332 | G/A | — | benign |
| rs1962965182 | 15:85,341,104 | A/G | — | uncertain significance |
| rs745925350 | 15:85,341,203 | G/A | — | uncertain significance |
| rs181448204 | 15:85,341,259 | G/C | — | likely benign |
| rs186188186 | 15:85,341,260 | C/A | — | uncertain significance |
| rs1329430021 | 15:85,341,267 | G/A | — | likely benign |
| rs2505664465 | 15:85,341,593 | A/G | — | uncertain significance |
| rs779210029 | 15:85,341,629 | C/T | — | uncertain significance |
| rs1009020534 | 15:85,341,640 | G/A | — | uncertain significance |
| rs139338244 | 15:85,341,669 | G/T | — | uncertain significance |
| rs201965611 | 15:85,341,673 | G/A | — | uncertain significance |
| rs1211858750 | 15:85,341,700 | G/A | — | uncertain significance |
| rs767121113 | 15:85,341,838 | G/A | — | uncertain significance |
| rs140752402 | 15:85,341,849 | G/A | — | uncertain significance |
| rs8182086 | 15:85,341,859 | G/A | — | benign |
| rs778336339 | 15:85,341,874 | C/T | — | likely benign |
| rs145494146 | 15:85,341,891 | C/T | — | uncertain significance |
| rs756945266 | 15:85,341,942 | C/T | — | uncertain significance |
| rs148855886 | 15:85,341,943 | G/A | — | uncertain significance |
| rs768744865 | 15:85,341,985 | C/T | — | uncertain significance |
| rs145238866 | 15:85,341,990 | C/T | — | benign |
| rs200921753 | 15:85,342,008 | C/T | — | uncertain significance |
| rs142580677 | 15:85,342,011 | C/T | — | uncertain significance |
| rs2505665743 | 15:85,342,024 | C/G | — | uncertain significance |
| rs1164234905 | 15:85,342,097 | C/A | — | uncertain significance |
| rs748149088 | 15:85,342,434 | A/G | — | uncertain significance |
| rs150829393 | 15:85,342,440 | G/A | missense variant | uncertain significance |
| rs146103176 | 15:85,343,113 | C/G | — | uncertain significance |
| rs768068244 | 15:85,343,194 | G/A | — | uncertain significance |
| rs111797492 | 15:85,345,133 | G/A | — | uncertain significance |
| rs756026866 | 15:85,345,154 | G/A | — | uncertain significance |
| rs1404849223 | 15:85,345,188 | T/A | — | uncertain significance |
| rs143259756 | 15:85,345,216 | C/T | — | benign |
| rs566303271 | 15:85,345,247 | A/G | — | uncertain significance |
| rs1596137692 | 15:85,345,253 | C/A | — | uncertain significance |
| rs557366252 | 15:85,345,389 | C/T | — | likely benign |
| rs759361603 | 15:85,345,392 | C/T | — | uncertain significance |
| rs146786916 | 15:85,345,510 | A/G | — | likely benign |
Showing 100 of 106 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.