SNHG29

Chr 17

small nucleolar RNA host gene 29

Also known as: ACIL, C17orf45, C17orf76-AS1, FAM211A-AS1, LRRC75A-AS1, NCRNA00188, TSAP19

NCBI Gene: 125144ENSG00000175061

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Jul 2025]

65
ClinVar variants
16
Pathogenic / LP
—
pLI score
0
Active trials
Clinical Summary— SNHG29
📋
ClinVar Variants
16 Pathogenic / Likely Pathogenic· 38 VUS of 65 total submissions

Population Genetics & Constraint

gnomAD

Constraint data not available from gnomAD.

ClinVar Variant Classifications

65 submitted variants in ClinVar

ClinVar

Classification Summary

Pathogenic16
VUS38
Likely Benign10
Benign1
16
Pathogenic
38
VUS
10
Likely Benign
1
Benign

Curated Variants Distribution

Classified variants from ClinVar · 5 ACMG categories

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
0
0
16
0
16
Likely Pathogenic
0
0
0
0
0
VUS
0
37
1
0
38
Likely Benign
0
8
0
2
10
Benign
0
1
0
0
1
Total04617265

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.

OMIM — Genotype-Phenotype

OMIM

No OMIM entries found.

Clinical Literature
Landmark / reviewRecent case evidence
Key Publications
Landmark & review papers · by relevance
PubMed
Top 10 resultsSearch PubMed ↗
Recent Gene-Specific Literature
Gene in title · MEDLINE · newest first
Europe PMC
Top 5 resultsSearch Europe PMC ↗

Clinical Trials

Active and recruiting trials from ClinicalTrials.gov

ClinicalTrials.gov

No active trials found for this gene.

Search ClinicalTrials.gov →

External Resources

Links to major genomics databases and tools