FGFBP2
fibroblast growth factor binding protein 2
Summary
This gene encodes a member of the fibroblast growth factor binding protein family. The encoded protein is a serum protein that is selectively secreted by cytotoxic lymphocytes and may be involved in cytotoxic lymphocyte-mediated immunity. An increase in the amount of gene product may be associated with atopic asthma and mild extrinsic asthma.[provided by RefSeq, Jan 2025]
Known Variants34 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs189427472 | 4:15,961,914 | C/T | downstream gene variant | — |
| rs1012199963 | 4:15,964,085 | C/G | — | uncertain significance |
| rs112278577 | 4:15,964,088 | C/T | — | likely benign |
| rs199734732 | 4:15,964,090 | G/T | — | uncertain significance |
| rs2474597271 | 4:15,964,137 | A/T | — | uncertain significance |
| rs1236207169 | 4:15,964,139 | T/C | — | uncertain significance |
| rs2474597276 | 4:15,964,146 | A/G | — | uncertain significance |
| rs780355175 | 4:15,964,167 | C/T | — | uncertain significance |
| rs749676676 | 4:15,964,168 | A/T | — | uncertain significance |
| rs151064854 | 4:15,964,176 | C/T | — | uncertain significance |
| rs145734233 | 4:15,964,214 | C/T | — | uncertain significance |
| rs376534161 | 4:15,964,238 | A/G | — | uncertain significance |
| rs546714840 | 4:15,964,281 | G/C | — | uncertain significance |
| rs1713120139 | 4:15,964,332 | G/C | — | uncertain significance |
| rs1713120668 | 4:15,964,346 | C/T | — | uncertain significance |
| rs1713122637 | 4:15,964,379 | T/C | — | uncertain significance |
| rs2474597675 | 4:15,964,385 | T/C | — | uncertain significance |
| rs772057742 | 4:15,964,407 | C/T | — | uncertain significance |
| rs201297539 | 4:15,964,424 | G/T | — | uncertain significance |
| rs765289147 | 4:15,964,428 | C/A | — | uncertain significance |
| rs137933914 | 4:15,964,439 | G/T | — | uncertain significance |
| rs142331717 | 4:15,964,451 | C/T | missense variant | — |
| rs573280165 | 4:15,964,452 | G/A | — | uncertain significance |
| rs748757540 | 4:15,964,458 | G/T | — | uncertain significance |
| rs772903611 | 4:15,964,487 | T/G | — | uncertain significance |
| rs747613275 | 4:15,964,563 | G/A | — | uncertain significance |
| rs62617788 | 4:15,964,574 | T/C | — | uncertain significance |
| rs765722115 | 4:15,964,587 | C/T | — | uncertain significance |
| rs531327066 | 4:15,964,617 | G/A | — | uncertain significance |
| rs1261207797 | 4:15,964,620 | T/C | — | uncertain significance |
| rs745626344 | 4:15,964,644 | T/C | — | uncertain significance |
| rs2474598235 | 4:15,964,700 | A/G | — | uncertain significance |
| rs74842426 | 4:15,964,812 | C/T | regulatory region variant | — |
| rs4698433 | 4:15,964,863 | G/A | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.