LGALS9C
galectin 9C
Summary
This gene was initially thought to represent a pseudogene of galectin 9; however, this transcript has good exon-intron structure and encodes a predicted protein of the same size as and highly similar to galectin 9. This gene is one of two similar loci on chromosome 17p similar to galectin 9 and now thought to be protein-encoding. This gene is the more telomeric gene. [provided by RefSeq, Jul 2008]
Known Variants25 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs551297983 | 17:18,379,637 | T/C | — | — |
| rs138868486 | 17:18,380,190 | G/C | — | likely benign |
| rs770825950 | 17:18,380,199 | C/A | — | uncertain significance |
| rs577572589 | 17:18,389,237 | C/T | intron variant | — |
| rs139721727 | 17:18,389,259 | A/C | — | uncertain significance |
| rs754982258 | 17:18,389,268 | C/T | — | uncertain significance |
| rs748067837 | 17:18,389,283 | A/T | — | uncertain significance |
| rs777029518 | 17:18,389,319 | A/G | — | uncertain significance |
| rs765706999 | 17:18,389,321 | G/A | — | uncertain significance |
| rs1269343833 | 17:18,389,402 | G/A | — | uncertain significance |
| rs1598147978 | 17:18,390,979 | C/T | — | likely benign |
| rs758797764 | 17:18,391,023 | C/A | — | uncertain significance |
| rs371253004 | 17:18,392,262 | G/T | — | uncertain significance |
| rs779017810 | 17:18,392,298 | C/T | — | uncertain significance |
| rs549798138 | 17:18,392,312 | G/A | — | uncertain significance |
| rs2508645260 | 17:18,395,838 | C/T | — | uncertain significance |
| rs999357487 | 17:18,396,061 | C/G | — | uncertain significance |
| rs373896961 | 17:18,396,068 | T/G | — | uncertain significance |
| rs1414110352 | 17:18,396,072 | G/A | — | uncertain significance |
| rs759117057 | 17:18,396,153 | G/A | — | uncertain significance |
| rs1989922444 | 17:18,397,535 | G/T | — | uncertain significance |
| rs1486960693 | 17:18,397,574 | G/A | — | uncertain significance |
| rs781370957 | 17:18,397,589 | G/A | — | uncertain significance |
| rs775117974 | 17:18,397,660 | G/C | — | uncertain significance |
| rs2508653811 | 17:18,397,677 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.