SFI1
SFI1 centrin binding protein
Summary
Enables phosphatase binding activity. Located in centriole. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants132 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2518134580 | 22:31,904,304 | A/T | — | uncertain significance |
| rs751815927 | 22:31,904,353 | T/C | — | uncertain significance |
| rs753679212 | 22:31,924,743 | G/T | — | uncertain significance |
| rs2518628323 | 22:31,924,746 | T/C | — | uncertain significance |
| rs529484779 | 22:31,924,758 | C/T | — | uncertain significance |
| rs747647817 | 22:31,924,759 | G/C | — | uncertain significance |
| rs770151236 | 22:31,924,774 | G/T | — | uncertain significance |
| rs16989698 | 22:31,924,798 | G/A | — | benign |
| rs2518629154 | 22:31,924,809 | A/G | — | likely benign |
| rs550696235 | 22:31,924,827 | C/T | — | uncertain significance |
| rs184362539 | 22:31,924,843 | G/T | — | uncertain significance |
| rs755312393 | 22:31,927,045 | T/G | — | uncertain significance |
| rs1041564046 | 22:31,927,071 | A/T | — | uncertain significance |
| rs78926500 | 22:31,941,067 | G/C | intron variant | — |
| rs775548328 | 22:31,942,855 | A/G | — | uncertain significance |
| rs768392322 | 22:31,942,864 | G/A | — | likely benign |
| rs2060145039 | 22:31,942,894 | A/C | — | uncertain significance |
| rs146504169 | 22:31,942,898 | G/C | — | uncertain significance |
| rs756112264 | 22:31,942,922 | G/T | — | uncertain significance |
| rs779406040 | 22:31,946,232 | C/T | — | likely benign |
| rs201319945 | 22:31,946,287 | G/A | — | likely benign |
| rs369986616 | 22:31,946,296 | A/G | — | likely benign |
| rs55807615 | 22:31,946,514 | C/T | intron variant | — |
| rs16989760 | 22:31,951,808 | A/G | upstream gene variant | — |
| rs369404082 | 22:31,952,965 | G/T | — | uncertain significance |
| rs753748915 | 22:31,953,044 | C/T | — | likely benign |
| rs764236180 | 22:31,957,314 | T/A | — | uncertain significance |
| rs201351749 | 22:31,957,317 | G/C | — | uncertain significance |
| rs201980284 | 22:31,957,326 | G/C | — | uncertain significance |
| rs2063118557 | 22:31,969,051 | C/T | — | uncertain significance |
| rs199812634 | 22:31,969,098 | G/A | — | uncertain significance |
| rs776367799 | 22:31,969,110 | G/A | — | uncertain significance |
| rs2063125123 | 22:31,969,132 | A/G | — | uncertain significance |
| rs750503268 | 22:31,969,152 | G/C | — | uncertain significance |
| rs374140512 | 22:31,969,192 | A/G | — | uncertain significance |
| rs2519899214 | 22:31,971,279 | G/A | — | uncertain significance |
| rs201900042 | 22:31,971,288 | C/T | — | uncertain significance |
| rs368043306 | 22:31,971,309 | C/T | — | likely benign |
| rs769372788 | 22:31,971,354 | C/T | — | uncertain significance |
| rs200708380 | 22:31,971,355 | G/A | — | uncertain significance |
| rs2519899827 | 22:31,971,375 | C/T | — | uncertain significance |
| rs144440001 | 22:31,972,728 | C/T | intron variant | — |
| rs372138017 | 22:31,974,370 | A/G | — | likely benign |
| rs1375109979 | 22:31,976,285 | A/G | — | uncertain significance |
| rs371915020 | 22:31,979,870 | A/G | — | uncertain significance |
| rs762410102 | 22:31,979,888 | C/T | — | likely benign |
| rs374895643 | 22:31,979,889 | G/A | — | likely benign |
| rs183680439 | 22:31,979,936 | C/G | — | uncertain significance |
| rs1467308733 | 22:31,979,939 | G/C | — | uncertain significance |
| rs757460080 | 22:31,981,079 | G/C | — | uncertain significance |
| rs769521093 | 22:31,981,092 | A/G | — | uncertain significance |
| rs371353301 | 22:31,981,119 | A/G | — | uncertain significance |
| rs753610155 | 22:31,985,455 | G/T | — | uncertain significance |
| rs2520686473 | 22:31,985,506 | T/C | — | uncertain significance |
| rs367598903 | 22:31,985,518 | G/A | — | likely benign |
| rs199525016 | 22:31,985,522 | C/A | — | likely benign |
| rs3986045 | 22:31,986,132 | G/C | — | — |
| rs2522162242 | 22:31,998,268 | G/A | — | uncertain significance |
| rs371619231 | 22:31,998,707 | C/T | — | uncertain significance |
| rs752234090 | 22:31,998,716 | C/T | — | uncertain significance |
| rs373091045 | 22:31,999,735 | C/T | — | likely benign |
| rs1385630117 | 22:31,999,779 | C/T | — | uncertain significance |
| rs777128215 | 22:31,999,801 | G/A | — | uncertain significance |
| rs765669240 | 22:32,000,308 | G/A | — | uncertain significance |
| rs540210849 | 22:32,000,319 | C/T | — | uncertain significance |
| rs2522307209 | 22:32,000,332 | T/C | — | uncertain significance |
| rs149899528 | 22:32,000,343 | C/T | — | likely benign |
| rs1197290341 | 22:32,000,349 | C/T | — | uncertain significance |
| rs559858464 | 22:32,000,360 | C/G | — | likely benign |
| rs2522308035 | 22:32,000,381 | G/C | — | uncertain significance |
| rs751011958 | 22:32,000,885 | C/T | — | uncertain significance |
| rs201405922 | 22:32,000,898 | C/A | — | uncertain significance |
| rs370776405 | 22:32,000,902 | G/C | — | uncertain significance |
| rs2068969023 | 22:32,002,332 | G/T | — | uncertain significance |
| rs753089246 | 22:32,002,352 | G/A | — | uncertain significance |
| rs764895114 | 22:32,003,953 | G/A | — | uncertain significance |
| rs145181683 | 22:32,007,137 | C/T | — | benign |
| rs371501095 | 22:32,007,150 | A/G | — | likely benign |
| rs768401003 | 22:32,007,152 | C/T | — | uncertain significance |
| rs368053809 | 22:32,007,170 | C/T | — | uncertain significance |
| rs200693435 | 22:32,007,224 | C/T | — | uncertain significance |
| rs558948334 | 22:32,007,225 | G/A | — | uncertain significance |
| rs377093919 | 22:32,007,251 | C/T | — | uncertain significance |
| rs369423375 | 22:32,007,252 | G/A | — | uncertain significance |
| rs1179895891 | 22:32,007,261 | C/T | — | likely benign |
| rs61743940 | 22:32,007,264 | A/T | — | likely benign |
| rs1372463101 | 22:32,007,284 | A/G | — | uncertain significance |
| rs752208935 | 22:32,007,801 | C/T | — | uncertain significance |
| rs58807171 | 22:32,008,200 | T/A | intron variant | — |
| rs372062054 | 22:32,009,156 | C/T | — | uncertain significance |
| rs755277133 | 22:32,009,182 | G/A | — | uncertain significance |
| rs2522794430 | 22:32,009,359 | C/T | — | uncertain significance |
| rs764353388 | 22:32,009,371 | A/G | — | uncertain significance |
| rs749047652 | 22:32,009,392 | G/A | — | uncertain significance |
| rs2070748946 | 22:32,009,403 | G/A | — | uncertain significance |
| rs2522795062 | 22:32,009,410 | A/G | — | uncertain significance |
| rs202074986 | 22:32,009,446 | C/T | — | uncertain significance |
| rs369378632 | 22:32,009,448 | C/T | — | uncertain significance |
| rs377278499 | 22:32,009,457 | C/T | — | uncertain significance |
| rs375385233 | 22:32,009,471 | C/T | — | likely benign |
Showing 100 of 132 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.