FHIP1A
FHF complex subunit HOOK interacting protein 1A
Summary
Involved in protein localization to perinuclear region of cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants99 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2724564 | 4:152,349,962 | G/T | intron variant | — |
| rs28622593 | 4:152,374,080 | A/C | — | — |
| rs6845395 | 4:152,403,605 | C/T | intron variant | — |
| rs111343306 | 4:152,437,994 | C/A | intron variant | — |
| rs6535803 | 4:152,441,914 | G/C | — | — |
| rs6814554 | 4:152,454,334 | G/A | intron variant | — |
| rs116521641 | 4:152,487,423 | G/A | — | likely benign |
| rs188418316 | 4:152,487,431 | C/T | — | uncertain significance |
| rs2546296642 | 4:152,487,487 | A/G | — | uncertain significance |
| rs199902938 | 4:152,498,602 | G/A | — | uncertain significance |
| rs746592641 | 4:152,498,686 | G/A | — | uncertain significance |
| rs553808969 | 4:152,498,723 | T/C | — | uncertain significance |
| rs1002716594 | 4:152,498,740 | G/A | — | uncertain significance |
| rs760778122 | 4:152,498,756 | C/T | — | uncertain significance |
| rs931040018 | 4:152,498,776 | T/G | — | uncertain significance |
| rs768487408 | 4:152,498,849 | A/C | — | uncertain significance |
| rs1397792310 | 4:152,498,860 | T/A | — | uncertain significance |
| rs200326017 | 4:152,498,875 | A/G | — | uncertain significance |
| rs907414867 | 4:152,498,882 | C/T | — | uncertain significance |
| rs756800958 | 4:152,498,906 | A/G | — | uncertain significance |
| rs543303426 | 4:152,498,945 | G/A | — | uncertain significance |
| rs1011656579 | 4:152,498,953 | A/T | — | uncertain significance |
| rs1431977820 | 4:152,499,043 | T/C | — | uncertain significance |
| rs1228196193 | 4:152,499,104 | C/T | — | uncertain significance |
| rs762607344 | 4:152,499,140 | C/T | — | uncertain significance |
| rs1170512409 | 4:152,499,148 | G/T | — | uncertain significance |
| rs138026287 | 4:152,499,205 | G/A | — | uncertain significance |
| rs376159656 | 4:152,499,210 | G/C | — | uncertain significance |
| rs947491028 | 4:152,499,214 | A/G | — | uncertain significance |
| rs756998700 | 4:152,499,224 | G/A | — | uncertain significance |
| rs959673485 | 4:152,507,817 | C/G | — | uncertain significance |
| rs542808503 | 4:152,507,889 | C/G | — | uncertain significance |
| rs745726262 | 4:152,507,898 | C/T | — | uncertain significance |
| rs1734232245 | 4:152,507,904 | C/A | — | uncertain significance |
| rs983011998 | 4:152,507,923 | C/T | — | uncertain significance |
| rs374535847 | 4:152,510,074 | A/G | — | uncertain significance |
| rs7695162 | 4:152,510,541 | G/T | — | — |
| rs1180045279 | 4:152,550,896 | C/T | — | uncertain significance |
| rs536110772 | 4:152,550,906 | G/A | — | uncertain significance |
| rs1169816700 | 4:152,550,917 | G/A | — | uncertain significance |
| rs200747616 | 4:152,550,918 | A/G | — | uncertain significance |
| rs749326371 | 4:152,550,969 | A/G | — | uncertain significance |
| rs754478645 | 4:152,550,989 | A/G | — | uncertain significance |
| rs376866022 | 4:152,550,996 | C/T | — | uncertain significance |
| rs369099144 | 4:152,551,019 | C/T | — | uncertain significance |
| rs954175830 | 4:152,559,854 | T/A | — | uncertain significance |
| rs17360371 | 4:152,565,374 | C/T | intron variant | — |
| rs188094362 | 4:152,567,726 | A/C | — | uncertain significance |
| rs370765283 | 4:152,567,767 | A/G | — | likely benign |
| rs1736809437 | 4:152,567,852 | C/A | — | uncertain significance |
| rs771761564 | 4:152,570,634 | G/A | — | uncertain significance |
| rs781115863 | 4:152,570,646 | G/A | — | uncertain significance |
| rs541223684 | 4:152,570,697 | C/A | — | uncertain significance |
| rs965461953 | 4:152,570,731 | G/A | — | likely benign |
| rs545503967 | 4:152,570,749 | G/A | — | uncertain significance |
| rs375182034 | 4:152,570,760 | G/A | — | uncertain significance |
| rs915855942 | 4:152,570,795 | G/A | — | uncertain significance |
| rs1736933017 | 4:152,570,803 | A/G | — | uncertain significance |
| rs564075271 | 4:152,570,812 | C/T | — | uncertain significance |
| rs376523990 | 4:152,570,830 | G/T | — | uncertain significance |
| rs199603138 | 4:152,570,833 | C/T | — | uncertain significance |
| rs567628337 | 4:152,570,857 | C/T | — | uncertain significance |
| rs2546405655 | 4:152,570,977 | C/T | — | uncertain significance |
| rs960126105 | 4:152,571,024 | A/C | — | uncertain significance |
| rs946715290 | 4:152,571,026 | T/G | — | uncertain significance |
| rs1366012179 | 4:152,571,030 | C/T | — | uncertain significance |
| rs369699317 | 4:152,571,037 | A/G | — | uncertain significance |
| rs894022529 | 4:152,571,160 | T/A | — | uncertain significance |
| rs1310293889 | 4:152,571,250 | G/C | — | uncertain significance |
| rs1476188905 | 4:152,571,253 | C/T | — | uncertain significance |
| rs778921797 | 4:152,571,332 | G/C | — | uncertain significance |
| rs2546406994 | 4:152,571,396 | G/T | — | uncertain significance |
| rs559558058 | 4:152,571,423 | G/A | — | uncertain significance |
| rs961354256 | 4:152,571,424 | C/T | — | uncertain significance |
| rs770265826 | 4:152,571,430 | C/T | — | uncertain significance |
| rs946926899 | 4:152,571,467 | C/G | — | uncertain significance |
| rs569849944 | 4:152,571,476 | G/C | — | uncertain significance |
| rs2546407595 | 4:152,571,577 | A/G | — | uncertain significance |
| rs766363756 | 4:152,571,610 | A/G | — | uncertain significance |
| rs373341384 | 4:152,571,631 | C/T | — | uncertain significance |
| rs768003391 | 4:152,571,682 | G/A | — | uncertain significance |
| rs780912010 | 4:152,571,709 | G/A | — | likely benign |
| rs72730114 | 4:152,571,730 | G/T | — | uncertain significance |
| rs2545904158 | 4:152,577,396 | G/T | — | uncertain significance |
| rs369125491 | 4:152,577,398 | G/A | — | uncertain significance |
| rs374875548 | 4:152,577,461 | G/A | — | uncertain significance |
| rs928570122 | 4:152,577,507 | C/T | — | uncertain significance |
| rs2545904574 | 4:152,577,525 | A/G | — | uncertain significance |
| rs140617452 | 4:152,577,526 | C/T | — | benign |
| rs1560825755 | 4:152,577,549 | G/A | — | uncertain significance |
| rs190146723 | 4:152,577,924 | G/A | — | uncertain significance |
| rs369369956 | 4:152,578,009 | G/A | — | uncertain significance |
| rs1011992687 | 4:152,583,763 | C/T | — | uncertain significance |
| rs994769484 | 4:152,583,772 | C/T | — | uncertain significance |
| rs541957794 | 4:152,583,790 | C/G | — | uncertain significance |
| rs1327162399 | 4:152,583,794 | T/C | — | uncertain significance |
| rs2545915090 | 4:152,583,795 | G/A | — | uncertain significance |
| rs1185925343 | 4:152,583,833 | T/A | — | uncertain significance |
| rs6816002 | 4:152,589,439 | G/A | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.