ZC3H13
zinc finger CCCH-type containing 13
Summary
Enables RNA binding activity. Involved in mRNA processing. Located in nuclear speck. Part of RNA N6-methyladenosine methyltransferase complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants103 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs17067486 | 13:46,533,098 | A/C | downstream gene variant | — |
| rs1336852496 | 13:46,538,036 | C/T | — | uncertain significance |
| rs759206705 | 13:46,538,088 | A/C | — | uncertain significance |
| rs143461574 | 13:46,538,118 | G/T | — | uncertain significance |
| rs147987923 | 13:46,538,138 | A/C | — | uncertain significance |
| rs752685699 | 13:46,539,447 | C/A | — | uncertain significance |
| rs1451805842 | 13:46,539,549 | T/C | — | uncertain significance |
| rs146239696 | 13:46,541,724 | C/G | — | uncertain significance |
| rs754217595 | 13:46,541,732 | G/T | — | uncertain significance |
| rs1952206605 | 13:46,541,792 | A/G | — | uncertain significance |
| rs748313690 | 13:46,541,919 | T/G | — | uncertain significance |
| rs1952221433 | 13:46,541,947 | T/C | — | uncertain significance |
| rs2548769660 | 13:46,542,013 | C/T | — | uncertain significance |
| rs374259305 | 13:46,542,046 | T/C | — | uncertain significance |
| rs1377400470 | 13:46,542,109 | C/T | — | uncertain significance |
| rs760886758 | 13:46,542,960 | C/T | — | uncertain significance |
| rs551063325 | 13:46,543,059 | C/T | — | uncertain significance |
| rs889890136 | 13:46,543,084 | G/A | — | uncertain significance |
| rs145846015 | 13:46,543,170 | G/A | — | uncertain significance |
| rs148627174 | 13:46,543,185 | A/G | — | likely benign |
| rs758977103 | 13:46,543,188 | C/T | — | uncertain significance |
| rs376194256 | 13:46,543,222 | T/C | — | uncertain significance |
| rs759678132 | 13:46,543,226 | A/G | — | likely benign |
| rs752781697 | 13:46,543,236 | T/C | — | uncertain significance |
| rs144601974 | 13:46,543,270 | T/C | — | uncertain significance |
| rs1461820271 | 13:46,543,306 | C/T | — | uncertain significance |
| rs375409144 | 13:46,543,318 | C/G | — | uncertain significance |
| rs141717640 | 13:46,543,416 | G/A | — | uncertain significance |
| rs371989753 | 13:46,543,519 | C/T | — | uncertain significance |
| rs761927323 | 13:46,543,539 | T/C | — | uncertain significance |
| rs2548788981 | 13:46,543,571 | T/C | — | uncertain significance |
| rs777332072 | 13:46,543,573 | T/C | — | uncertain significance |
| rs749002051 | 13:46,543,575 | G/T | — | uncertain significance |
| rs866544730 | 13:46,543,615 | C/T | — | uncertain significance |
| rs2548790450 | 13:46,543,710 | T/G | — | uncertain significance |
| rs1396023666 | 13:46,543,713 | C/A | — | uncertain significance |
| rs2548790521 | 13:46,543,716 | T/C | — | uncertain significance |
| rs763455781 | 13:46,543,735 | T/C | — | uncertain significance |
| rs751139064 | 13:46,543,737 | T/A | — | uncertain significance |
| rs779826371 | 13:46,543,756 | C/A | — | uncertain significance |
| rs1348533894 | 13:46,543,960 | C/T | — | uncertain significance |
| rs761376101 | 13:46,543,968 | C/T | — | uncertain significance |
| rs2548793661 | 13:46,544,007 | T/G | — | uncertain significance |
| rs571568435 | 13:46,544,043 | G/A | — | uncertain significance |
| rs768998182 | 13:46,544,058 | C/T | — | uncertain significance |
| rs776022362 | 13:46,544,517 | T/C | — | uncertain significance |
| rs140219290 | 13:46,544,568 | G/A | — | uncertain significance |
| rs997438487 | 13:46,544,592 | T/C | — | uncertain significance |
| rs2548799665 | 13:46,544,596 | G/A | — | uncertain significance |
| rs779722592 | 13:46,549,463 | C/T | — | uncertain significance |
| rs768776672 | 13:46,549,475 | C/T | — | uncertain significance |
| rs746861762 | 13:46,549,751 | G/A | — | uncertain significance |
| rs1952975899 | 13:46,549,775 | T/C | — | uncertain significance |
| rs749159735 | 13:46,549,820 | C/T | — | uncertain significance |
| rs372572635 | 13:46,549,832 | C/A | — | uncertain significance |
| rs771366829 | 13:46,549,920 | G/A | — | uncertain significance |
| rs139890974 | 13:46,553,958 | G/C | — | uncertain significance |
| rs537119782 | 13:46,553,966 | G/A | — | uncertain significance |
| rs2548855571 | 13:46,554,015 | A/C | — | uncertain significance |
| rs920548097 | 13:46,554,042 | A/C | — | uncertain significance |
| rs201681294 | 13:46,554,064 | C/T | — | uncertain significance |
| rs1189213048 | 13:46,554,083 | G/A | — | uncertain significance |
| rs1414888440 | 13:46,559,602 | C/T | — | uncertain significance |
| rs1025942396 | 13:46,559,608 | G/C | — | uncertain significance |
| rs745791047 | 13:46,559,623 | C/T | — | uncertain significance |
| rs752031871 | 13:46,559,780 | G/A | — | uncertain significance |
| rs368245456 | 13:46,559,808 | A/T | — | uncertain significance |
| rs200763938 | 13:46,563,002 | C/G | — | uncertain significance |
| rs374911102 | 13:46,563,024 | T/C | — | uncertain significance |
| rs1052767529 | 13:46,563,068 | G/A | — | uncertain significance |
| rs768432304 | 13:46,563,095 | C/T | — | uncertain significance |
| rs11537603 | 13:46,563,128 | C/A | — | uncertain significance |
| rs752098751 | 13:46,563,197 | A/G | — | uncertain significance |
| rs192073528 | 13:46,563,990 | T/C | regulatory region variant | — |
| rs141399987 | 13:46,565,216 | C/A | intron variant | — |
| rs189703993 | 13:46,570,339 | G/A | intron variant | — |
| rs150387526 | 13:46,574,113 | T/C | intron variant | — |
| rs2548990353 | 13:46,577,284 | C/A | — | uncertain significance |
| rs147013113 | 13:46,577,301 | C/T | — | uncertain significance |
| rs138164827 | 13:46,577,316 | C/T | — | uncertain significance |
| rs374130519 | 13:46,577,321 | G/T | — | uncertain significance |
| rs763237553 | 13:46,577,338 | T/C | — | uncertain significance |
| rs774373778 | 13:46,577,407 | G/C | — | uncertain significance |
| rs199537193 | 13:46,577,416 | G/T | — | uncertain significance |
| rs2548992139 | 13:46,577,431 | T/C | — | uncertain significance |
| rs766819940 | 13:46,577,434 | G/A | — | uncertain significance |
| rs200633604 | 13:46,584,535 | T/C | — | uncertain significance |
| rs751291240 | 13:46,584,549 | G/A | — | uncertain significance |
| rs140179398 | 13:46,584,567 | C/T | — | uncertain significance |
| rs201401739 | 13:46,584,606 | G/A | — | uncertain significance |
| rs9534280 | 13:46,585,051 | T/G | — | — |
| rs754743826 | 13:46,585,630 | G/T | — | uncertain significance |
| rs2549046145 | 13:46,585,674 | T/C | — | uncertain significance |
| rs142122681 | 13:46,594,608 | C/T | — | uncertain significance |
| rs2549096588 | 13:46,594,625 | T/C | — | uncertain significance |
| rs9534288 | 13:46,605,441 | T/C | intron variant | — |
| rs7318648 | 13:46,606,632 | T/A | — | — |
| rs575603783 | 13:46,608,995 | T/A | — | — |
| rs199639834 | 13:46,616,321 | T/G | — | uncertain significance |
| rs1453640206 | 13:46,619,107 | A/G | — | likely benign |
Showing 100 of 103 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.