Gene

SPEN

SPEN is a gene. This site has 24 published variants inside it, each from a published genetic study, joining it to 5 condition pages.

Conditions it is linked to

Variants inside SPEN (24)

rs2071243064 · Autism spectrum disorder
rs35514973 · Benign nodular goiter
rs139816220 · CTRC protein levels
rs537231104 · EPHA2 protein levels
rs6701290 · Heel bone mineral density
rs848209 · Hemoglobin levels
rs2071205857 · Inborn genetic diseases
rs2522927850 · Inborn genetic diseases
rs770680602 · Inborn genetic diseases
rs1386910185 · Radio-Tartaglia syndrome
rs1399970491 · Radio-Tartaglia syndrome
rs2070991188 · Radio-Tartaglia syndrome
rs2071187754 · Radio-Tartaglia syndrome
rs2071203144 · Radio-Tartaglia syndrome
rs2148739431 · Radio-Tartaglia syndrome
rs2148741741 · Radio-Tartaglia syndrome
rs2522936339 · Radio-Tartaglia syndrome
rs2523080343 · Radio-Tartaglia syndrome
rs2523081142 · Radio-Tartaglia syndrome
rs752207572 · Radio-Tartaglia syndrome
rs769218008 · Radio-Tartaglia syndrome
rs772105874 · Radio-Tartaglia syndrome
rs2148742017 · SPEN-related disorder
rs2523072296 · SPEN-related disorder

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

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

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

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.