Gene

REST

REST is a gene. This site has 22 published variants inside it and 12 near it, each from a published genetic study, joining it to 8 condition pages.

Conditions it is linked to

Variants inside REST (22)

rs1720770872 · Autosomal dominant nonsyndromic hearing loss 27
rs2109573013 · Autosomal dominant nonsyndromic hearing loss 27
rs2140147 · Body mass index
rs6554401 · Cell adhesion molecule 3 levels
rs7680140 · Externalizing behaviour (multivariate analysis)
rs1553904077 · Fibromatosis, gingival, 1
rs1284461687 · Fibromatosis, gingival, 5
rs2475854474 · Fibromatosis, gingival, 5
rs1708751 · Forced expiratory volume (baseline)
rs17087265 · Height
rs781663 · Height
rs61748757 · Height (baseline)
rs10020462 · IDP T1 FAST ROIs R cerebellum VIIb
rs781659 · Impedance of arm right (UKB data field 23109)
rs1553904378 · Inborn genetic diseases
rs12645070 · Mean platelet volume
rs56155140 · Osteoarthritis (with total hip replacement)
rs3796529 · Platelet count
rs55879786 · Platelet crit (UKB data field 30090)
rs9684742 · Risk-taking tendency (4-domain principal component model)
rs1961950 · SEZ6L2 protein levels
rs115656299 · SPINK2 protein levels

Variants near REST (12)

Positions outside the gene, filed under it because it is the closest. A variant near a gene does not always act through it.

rs56281640 · Alanine aminotransferase levels
rs6857226 · Cortical surface area
rs62308110 · Eosinophil count
rs62308111 · Eosinophil count
rs12510703 · Height
rs143898047 · Kidney cortex volume
rs67043033 · mean corpuscular volume (MCV, minimum, inv-norm transformed)
rs56162812 · Mean platelet volume
rs55762216 · Platelet count
rs2412771 · Red cell distribution width
rs193262424 · SPINK2 protein levels
rs13116564 · Vertex-wise sulcal depth

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

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

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.