ZFYVE19
zinc finger FYVE-type containing 19
Summary
Enables phosphatidylinositol-3-phosphate binding activity. Involved in midbody abscission; mitotic cytokinesis checkpoint signaling; and negative regulation of cytokinesis. Located in centrosome; cleavage furrow; and midbody. Implicated in progressive familial intrahepatic cholestasis. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants41 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs376938566 | 15:41,099,797 | G/A | — | uncertain significance |
| rs534190263 | 15:41,099,813 | C/G | — | uncertain significance |
| rs767863077 | 15:41,099,894 | G/A | — | uncertain significance |
| rs926447940 | 15:41,099,912 | G/A | — | uncertain significance |
| rs749863222 | 15:41,099,926 | G/A | — | uncertain significance |
| rs754910861 | 15:41,099,990 | A/T | — | uncertain significance |
| rs1215965232 | 15:41,100,013 | A/G | — | pathogenic |
| rs761078822 | 15:41,100,040 | G/A | — | uncertain significance |
| rs769683740 | 15:41,101,351 | C/G | — | pathogenic |
| rs370488168 | 15:41,101,375 | C/T | — | likely benign |
| rs2504718272 | 15:41,101,411 | G/A | — | uncertain significance |
| rs1890395046 | 15:41,101,416 | C/T | — | pathogenic |
| rs1890395882 | 15:41,101,422 | C/T | — | uncertain significance |
| rs750719747 | 15:41,101,620 | A/G | — | likely benign |
| rs140044253 | 15:41,101,650 | A/C | — | uncertain significance |
| rs753378311 | 15:41,102,052 | G/C | — | uncertain significance |
| rs753989803 | 15:41,102,111 | C/T | — | pathogenic |
| rs566729022 | 15:41,102,126 | A/T | — | uncertain significance |
| rs769849615 | 15:41,102,136 | G/A | — | uncertain significance |
| rs771251472 | 15:41,102,144 | C/T | — | pathogenic |
| rs199947417 | 15:41,102,150 | C/T | — | conflicting classifications of pathogenicity |
| rs200940591 | 15:41,102,301 | C/T | — | uncertain significance |
| rs368589091 | 15:41,102,317 | A/C | — | uncertain significance |
| rs772689163 | 15:41,102,325 | C/T | — | uncertain significance |
| rs2504722037 | 15:41,102,356 | T/G | — | uncertain significance |
| rs375497733 | 15:41,102,364 | C/T | — | pathogenic |
| rs61734894 | 15:41,102,847 | G/A | — | uncertain significance |
| rs533156538 | 15:41,102,889 | C/A | — | likely benign |
| rs747007341 | 15:41,102,892 | G/A | — | uncertain significance |
| rs776500976 | 15:41,102,902 | C/T | — | uncertain significance |
| rs746090607 | 15:41,105,032 | C/T | — | uncertain significance |
| rs690347 | 15:41,105,926 | T/A | missense variant | — |
| rs2504731651 | 15:41,105,927 | C/A | — | uncertain significance |
| rs34516375 | 15:41,105,942 | G/A | — | likely benign |
| rs1409438432 | 15:41,105,966 | A/T | — | uncertain significance |
| rs527739568 | 15:41,105,968 | G/C | — | uncertain significance |
| rs779395187 | 15:41,105,974 | C/T | — | likely pathogenic |
| rs200306997 | 15:41,105,975 | G/A | — | likely benign |
| rs72735636 | 15:41,105,992 | C/T | — | likely benign |
| rs1403218797 | 15:41,106,228 | G/A | — | uncertain significance |
| rs768102426 | 15:41,106,254 | T/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.