FSIP1
fibrous sheath interacting protein 1
Summary
Predicted to act upstream of or within several processes, including axoneme assembly; homeostasis of number of cells within a tissue; and vesicle organization. Predicted to be active in acrosomal vesicle; nucleus; and sperm head. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants45 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs866552400 | 15:39,909,951 | C/T | — | uncertain significance |
| rs71472405 | 15:39,909,953 | G/A | — | uncertain significance |
| rs759738449 | 15:39,909,990 | G/A | — | uncertain significance |
| rs138630370 | 15:39,910,014 | G/C | — | uncertain significance |
| rs929238289 | 15:39,910,026 | A/G | — | uncertain significance |
| rs144527032 | 15:39,910,063 | C/T | — | likely benign |
| rs866086807 | 15:39,910,158 | T/G | — | uncertain significance |
| rs144954858 | 15:39,910,203 | C/T | — | likely benign |
| rs2504399491 | 15:39,910,394 | T/G | — | uncertain significance |
| rs10152640 | 15:39,910,431 | A/G | missense variant | — |
| rs7169574 | 15:39,916,517 | G/C | intron variant | — |
| rs72725098 | 15:39,932,973 | G/T | — | — |
| rs12899753 | 15:39,950,652 | C/G | intron variant | — |
| rs8034885 | 15:39,953,061 | C/T | intron variant | — |
| rs549166815 | 15:39,975,368 | C/A | — | — |
| rs2504698244 | 15:40,005,681 | C/A | — | uncertain significance |
| rs145334356 | 15:40,005,697 | T/C | — | likely benign |
| rs182307290 | 15:40,005,731 | T/A | — | benign |
| rs143010590 | 15:40,005,755 | T/C | — | uncertain significance |
| rs1189130900 | 15:40,005,762 | T/G | — | likely benign |
| rs536201152 | 15:40,018,800 | C/T | — | likely benign |
| rs145632918 | 15:40,018,870 | C/T | — | uncertain significance |
| rs772114003 | 15:40,018,875 | T/G | — | uncertain significance |
| rs765118693 | 15:40,018,945 | C/A | — | uncertain significance |
| rs572041423 | 15:40,030,371 | A/G | — | uncertain significance |
| rs2504785300 | 15:40,031,877 | T/C | — | uncertain significance |
| rs2504785718 | 15:40,031,938 | T/A | — | uncertain significance |
| rs1180689972 | 15:40,031,942 | T/C | — | uncertain significance |
| rs371733198 | 15:40,031,978 | T/C | — | uncertain significance |
| rs78959490 | 15:40,034,007 | T/G | — | uncertain significance |
| rs554134584 | 15:40,034,011 | T/C | — | likely benign |
| rs748369342 | 15:40,034,035 | T/C | — | uncertain significance |
| rs77162552 | 15:40,035,452 | G/A | intron variant | — |
| rs8033957 | 15:40,038,433 | T/G | — | — |
| rs1360374697 | 15:40,057,830 | C/A | — | uncertain significance |
| rs768046700 | 15:40,062,637 | C/G | — | uncertain significance |
| rs1295809903 | 15:40,062,675 | T/C | — | uncertain significance |
| rs1897844734 | 15:40,062,718 | C/T | — | uncertain significance |
| rs763028551 | 15:40,062,726 | T/A | — | uncertain significance |
| rs1001075268 | 15:40,062,766 | C/T | — | uncertain significance |
| rs369173704 | 15:40,062,783 | C/G | — | uncertain significance |
| rs145460504 | 15:40,062,808 | C/T | — | uncertain significance |
| rs1565560 | 15:40,062,825 | C/A | — | benign |
| rs759239988 | 15:40,068,641 | C/G | — | uncertain significance |
| rs369384375 | 15:40,068,700 | T/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.