ZBTB17
zinc finger and BTB domain containing 17
Summary
This gene encodes a zinc finger protein involved in the regulation of c-myc. The symbol MIZ1 has also been associated with PIAS2 which is a different gene located on chromosome 18. [provided by RefSeq, Jul 2008]
Known Variants54 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1287184446 | 1:16,268,495 | G/A | — | uncertain significance |
| rs1335532943 | 1:16,268,622 | C/T | — | uncertain significance |
| rs147516539 | 1:16,268,644 | C/T | — | likely benign |
| rs2523122552 | 1:16,268,654 | G/A | — | uncertain significance |
| rs762057725 | 1:16,268,666 | C/T | — | uncertain significance |
| rs1570089711 | 1:16,268,741 | T/C | — | uncertain significance |
| rs72885816 | 1:16,268,784 | C/T | — | benign |
| rs376259268 | 1:16,268,817 | C/T | — | likely benign |
| rs2523125181 | 1:16,268,871 | G/C | — | uncertain significance |
| rs775686038 | 1:16,269,032 | T/C | — | uncertain significance |
| rs201524531 | 1:16,269,040 | G/C | — | benign |
| rs2523130191 | 1:16,269,190 | G/T | — | uncertain significance |
| rs751685396 | 1:16,269,685 | C/T | — | uncertain significance |
| rs4661672 | 1:16,269,737 | C/T | — | benign |
| rs2523138487 | 1:16,269,931 | C/T | — | uncertain significance |
| rs150689825 | 1:16,269,946 | C/T | — | uncertain significance |
| rs2523138897 | 1:16,269,966 | G/A | — | uncertain significance |
| rs777259857 | 1:16,269,994 | C/G | — | uncertain significance |
| rs201683775 | 1:16,270,394 | T/C | — | likely benign |
| rs1350282418 | 1:16,270,838 | T/C | — | uncertain significance |
| rs927212848 | 1:16,271,000 | C/T | — | uncertain significance |
| rs12134932 | 1:16,271,156 | C/A | — | benign |
| rs113384692 | 1:16,271,167 | G/A | — | benign |
| rs848216 | 1:16,271,180 | C/T | — | benign |
| rs2523156089 | 1:16,271,249 | T/C | — | uncertain significance |
| rs9661939 | 1:16,271,260 | G/A | — | benign |
| rs2523160983 | 1:16,271,542 | C/T | — | likely benign |
| rs747585610 | 1:16,271,596 | A/G | — | likely benign |
| rs1055926542 | 1:16,272,240 | C/T | — | uncertain significance |
| rs368013740 | 1:16,272,247 | T/C | — | likely benign |
| rs848217 | 1:16,272,250 | G/A | — | benign |
| rs1008918296 | 1:16,272,293 | G/A | — | uncertain significance |
| rs759468700 | 1:16,272,308 | G/A | — | uncertain significance |
| rs9429277 | 1:16,272,409 | C/T | — | benign |
| rs377672932 | 1:16,272,673 | C/T | — | uncertain significance |
| rs545852303 | 1:16,272,676 | C/T | — | uncertain significance |
| rs765796064 | 1:16,272,677 | G/A | — | likely benign |
| rs149712043 | 1:16,272,678 | C/T | — | uncertain significance |
| rs763520387 | 1:16,272,679 | G/A | — | uncertain significance |
| rs1236417292 | 1:16,272,685 | C/G | — | uncertain significance |
| rs201522658 | 1:16,272,694 | C/T | — | uncertain significance |
| rs147654293 | 1:16,272,752 | G/A | — | likely benign |
| rs2523177748 | 1:16,272,767 | C/G | — | uncertain significance |
| rs1188393328 | 1:16,272,780 | T/C | — | uncertain significance |
| rs112062500 | 1:16,272,806 | G/A | — | benign |
| rs200322992 | 1:16,272,819 | T/C | — | likely benign |
| rs61782258 | 1:16,272,933 | A/C | — | benign |
| rs145800378 | 1:16,273,489 | T/A | — | uncertain significance |
| rs776892143 | 1:16,273,524 | T/G | — | uncertain significance |
| rs698891 | 1:16,274,769 | C/T | — | benign |
| rs150759933 | 1:16,274,831 | C/T | — | uncertain significance |
| rs377271800 | 1:16,274,981 | G/T | — | uncertain significance |
| rs112121101 | 1:16,275,052 | C/T | — | benign |
| rs10927875 | 1:16,299,312 | C/T | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.