SNHG29
Chr 17small nucleolar RNA host gene 29
Also known as: ACIL, C17orf45, C17orf76-AS1, FAM211A-AS1, LRRC75A-AS1, NCRNA00188, TSAP19
SNHG29 encodes a small nucleolar RNA host gene predicted to be involved in RNA processing within the nucleolus. Currently, no established human diseases have been definitively linked to mutations in this gene. The clinical significance and inheritance pattern remain to be determined as pathogenic variants have not been well-characterized.
Population Genetics & Constraint
Constraint data not available from gnomAD.
ClinVar Variant Classifications
67 submitted variants in ClinVar
Classification Summary
Curated Variants Distribution
Classified variants from ClinVar · 5 ACMG categories
| Classification | LoF | Missense + Inframe | Non-coding | Synonymous | Total |
|---|---|---|---|---|---|
Pathogenic | 0 | 0 | 16 | 0 | 16 |
Likely Pathogenic | 0 | 0 | 0 | 0 | 0 |
VUS | 0 | 37 | 1 | 0 | 38 |
Likely Benign | 1 | 8 | 0 | 1 | 10 |
Benign | 0 | 1 | 0 | 0 | 1 |
| Total | 1 | 46 | 17 | 1 | 65 |
LoF = frameshift, stop gained/lost, canonical splice · Counts from ClinVar esearch · Updated hourly
View in ClinVar →Protein Context — Lollipop Plot
SNHG29 · protein map & ClinVar variants
Showing all ClinVar variants across the protein. Search a specific variant to highlight its position.
3D Protein StructureAlphaFold
External Resources
Links to major genomics databases and tools
Clinical Trials
Active and recruiting trials from ClinicalTrials.gov
No active trials found for this gene.
Search ClinicalTrials.gov →External Resources
Links to major genomics databases and tools