POTEH
POTE ankyrin domain family member H
Summary
Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants34 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs758721146 | 22:16,258,221 | C/T | — | uncertain significance |
| rs199586979 | 22:16,258,285 | A/T | — | likely benign |
| rs769823793 | 22:16,258,302 | C/T | — | uncertain significance |
| rs10154680 | 22:16,266,964 | C/T | — | likely benign |
| rs779170078 | 22:16,266,968 | C/A | — | uncertain significance |
| rs747696924 | 22:16,267,058 | A/G | — | uncertain significance |
| rs2517121708 | 22:16,269,886 | T/C | — | uncertain significance |
| rs576834108 | 22:16,275,272 | C/T | — | uncertain significance |
| rs2517113441 | 22:16,277,782 | C/T | — | uncertain significance |
| rs1464662509 | 22:16,282,159 | C/T | — | uncertain significance |
| rs4497955 | 22:16,282,315 | C/T | — | likely benign |
| rs775617123 | 22:16,287,329 | C/G | — | uncertain significance |
| rs762153495 | 22:16,287,368 | C/T | — | uncertain significance |
| rs371550897 | 22:16,287,369 | G/A | — | uncertain significance |
| rs757877748 | 22:16,287,374 | T/C | — | uncertain significance |
| rs1397959333 | 22:16,287,400 | G/T | — | uncertain significance |
| rs200405088 | 22:16,287,431 | T/C | — | likely benign |
| rs550458702 | 22:16,287,445 | C/A | — | uncertain significance |
| rs568761899 | 22:16,287,449 | C/A | — | uncertain significance |
| rs766101138 | 22:16,287,467 | C/T | — | uncertain significance |
| rs200923174 | 22:16,287,557 | C/G | — | uncertain significance |
| rs1989269862 | 22:16,287,566 | G/A | — | uncertain significance |
| rs368386347 | 22:16,287,608 | G/C | — | uncertain significance |
| rs200416250 | 22:16,287,678 | G/A | — | uncertain significance |
| rs2517101715 | 22:16,287,689 | C/G | — | uncertain significance |
| rs376654571 | 22:16,287,694 | C/G | — | uncertain significance |
| rs1183690272 | 22:16,287,703 | C/A | — | uncertain significance |
| rs747485524 | 22:16,287,735 | C/T | — | uncertain significance |
| rs750280796 | 22:16,287,746 | C/T | — | uncertain significance |
| rs372662805 | 22:16,287,752 | G/C | — | uncertain significance |
| rs544319673 | 22:16,287,786 | A/C | — | uncertain significance |
| rs199665763 | 22:16,287,800 | C/T | — | uncertain significance |
| rs754460373 | 22:16,287,801 | G/A | — | likely benign |
| rs536930974 | 22:16,289,925 | A/G | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.