SNORA6

Chr 3

small nucleolar RNA, H/ACA box 6

Also known as: ACA6

SNORA6 encodes a small nucleolar RNA predicted to be involved in RNA processing within the nucleolus. Current databases do not report established disease associations or inheritance patterns for this gene. Clinical significance of SNORA6 variants in pediatric neurological conditions remains to be determined.

ResearchSummary from RefSeq
Clinical SummarySNORA6
📋
ClinVar Variants
3 unique Pathogenic / Likely Pathogenic of 3 total submissions

Population Genetics & Constraint

Constraint data not available from gnomAD.

ClinVar Variant Classifications

3 submitted variants in ClinVar

Classification Summary

Pathogenic3
3
Pathogenic

Curated Variants Distribution

Classified variants from ClinVar · 5 ACMG categories· variant type breakdown unavailable

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
3
Likely Pathogenic
0
VUS
0
Likely Benign
0
Benign
0
Total3

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

SNORA6 · protein map & ClinVar variants

Showing all ClinVar variants across the protein. Search a specific variant to highlight its position.

3D Protein StructureAlphaFold

Clinical Trials

Active and recruiting trials from ClinicalTrials.gov

No active trials found for this gene.

Search ClinicalTrials.gov →
Clinical Literature
Open Research Assistant →
Full-Text Mentions
NLP-detected gene mentions in article bodies · via PubTator3
PubTator3
Top 5 full-text resultsSearch PubTator3 ↗
Key Publications
Landmark & review papers · by relevance
PubMed
Top 1 results · since 2015Search PubMed ↗
Recent Gene-Specific Literature
Gene in title · MEDLINE · newest first
Europe PMC

No open access results found