SIGLEC7
sialic acid binding Ig like lectin 7
Summary
Predicted to enable sialic acid binding activity. Predicted to be involved in cell adhesion. Predicted to be located in membrane. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants34 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs144363592 | 19:51,645,726 | G/A | missense variant | — |
| rs539442902 | 19:51,645,754 | A/C | — | uncertain significance |
| rs1667885069 | 19:51,645,760 | G/A | — | uncertain significance |
| rs2513840300 | 19:51,645,772 | C/G | — | uncertain significance |
| rs148480141 | 19:51,645,901 | G/A | — | uncertain significance |
| rs755904310 | 19:51,645,915 | C/T | — | uncertain significance |
| rs771229132 | 19:51,645,979 | C/T | — | uncertain significance |
| rs533294268 | 19:51,646,053 | G/A | — | uncertain significance |
| rs766163463 | 19:51,647,723 | A/G | — | uncertain significance |
| rs1261561128 | 19:51,647,737 | G/A | — | uncertain significance |
| rs577893614 | 19:51,647,758 | G/A | — | uncertain significance |
| rs150924967 | 19:51,647,762 | C/T | — | uncertain significance |
| rs114209391 | 19:51,647,770 | A/G | — | benign |
| rs144612094 | 19:51,647,821 | C/T | — | uncertain significance |
| rs549102934 | 19:51,647,859 | C/G | — | uncertain significance |
| rs117714252 | 19:51,647,925 | C/G | — | uncertain significance |
| rs528134634 | 19:51,648,931 | T/C | — | — |
| rs2092104581 | 19:51,649,156 | G/C | — | uncertain significance |
| rs1364722668 | 19:51,650,018 | G/A | — | uncertain significance |
| rs771104179 | 19:51,650,044 | G/C | — | uncertain significance |
| rs201978572 | 19:51,650,052 | G/A | — | uncertain significance |
| rs2513848710 | 19:51,650,095 | T/A | — | uncertain significance |
| rs2513849455 | 19:51,650,507 | G/A | — | uncertain significance |
| rs139160664 | 19:51,650,521 | G/A | — | uncertain significance |
| rs567788684 | 19:51,650,550 | C/G | — | uncertain significance |
| rs200528542 | 19:51,650,563 | T/C | — | uncertain significance |
| rs2513849638 | 19:51,650,573 | A/G | — | uncertain significance |
| rs141544900 | 19:51,652,994 | T/C | downstream gene variant | — |
| rs188809440 | 19:51,654,157 | C/T | downstream gene variant | — |
| rs192872396 | 19:51,654,582 | G/T | downstream gene variant | — |
| rs771779160 | 19:51,656,329 | A/T | — | uncertain significance |
| rs764338247 | 19:51,656,420 | G/A | — | uncertain significance |
| rs201414205 | 19:51,656,430 | G/C | — | uncertain significance |
| rs542015089 | 19:51,656,468 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.