TMEM92 Chromosome 17

Transmembrane protein 92
1 variant 1 Health Risk

Upload your DNA to see your personal genotypes for variants in TMEM92.

What This Gene Does
Located in nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Associated Conditions (4)
Global developmental delay
Cerebellar atrophy
Bilateral squint
Hydrocephalus
Key Variants
RS730882247
Likely pathogenic
Global developmental delay, Cerebellar atrophy, Bilateral squint
Health Risk
All Variants (1)
RSID Category Clinical Significance Conditions
RS730882247 Health Risk Likely pathogenic Global developmental delay, Cerebellar atrophy, Bilateral squint
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