Gene

SPC25

SPC25 is a gene. This site has 30 published variants inside it, each from a published genetic study, joining it to 7 condition pages.

Conditions it is linked to

Variants inside SPC25 (30)

rs12475700 · Aspartate aminotransferase (AST, minimum, inv-norm transformed)
rs62176784 · Aspartate aminotransferase levels (UKB data field 30650)
rs112438419 · Blood glucose levels
rs13430620 · Blood glucose levels
rs2232315 · Blood glucose levels
rs2232323 · Blood glucose levels
rs2232328 · Blood glucose levels
rs76372731 · Blood glucose levels
rs78573157 · Blood glucose levels
rs13431652 · Cardiovascular-kidney-metabolic syndrome candidate subtype 28
rs13387347 · Fasting blood glucose
rs145353824 · Fasting glucose
rs492594 · Fasting glucose
rs7582529 · Fasting glucose
rs115128825 · Glucose levels (UKB data field 30740)
rs141806587 · Glucose levels (UKB data field 30740)
rs146779637 · Glucose levels (UKB data field 30740)
rs201647518 · Glucose levels (UKB data field 30740)
rs2232324 · Glucose levels (UKB data field 30740)
rs71430652 · Glucose levels (UKB data field 30740)
rs150171632 · Glycated hemoglobin levels
rs151057583 · Glycated hemoglobin levels
rs12993143 · Height (baseline)
rs12053049 · Hemoglobin A1c levels
rs526418 · Lymphocyte count
rs524586 · Mean platelet volume
rs143869345 · Random glucose levels
rs2140046 · Triglycerides to Total Lipids in Very Large HDL percentage
rs483109 · White blood cell count
rs35962426 · Whole body fat free mass (UKB data field 23101)

See SPC25 with everything it connects to on the Gene Knowledge Graph, or as data at /api/v1/genes/SPC25.

Quoting this page

Licensed CC BY-NC 4.0: free to read, share and adapt for non-commercial use, naming MyGeneLog™ and linking the exact page. Commercial use, including training or serving a commercial AI system, needs a licence — https://www.mygenelog.com/license

SPC25 gene. MyGeneLog™. https://www.mygenelog.com/genes/SPC25

A gene page gathers published research; it is not a test result and not medical advice. If a gene matters to your health, talk to a doctor or a genetic counsellor.