SNORA7A

Chr 3

small nucleolar RNA, H/ACA box 7A

Also known as: ACA7

SNORA7A encodes a small nucleolar RNA predicted to be involved in RNA processing within the nucleolus. Currently, no specific diseases have been definitively associated with mutations in this gene, and the inheritance pattern remains undetermined. The clinical significance of variants in SNORA7A requires further investigation.

ResearchSummary from RefSeq
Clinical SummarySNORA7A
📋
ClinVar Variants
9 unique Pathogenic / Likely Pathogenic· 1 VUS of 10 total submissions

Population Genetics & Constraint

Constraint data not available from gnomAD.

ClinVar Variant Classifications

10 submitted variants in ClinVar

Classification Summary

Pathogenic9
VUS1
9
Pathogenic
1
VUS

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
9
Likely Pathogenic
0
VUS
1
Likely Benign
0
Benign
0
Total10

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

SNORA7A · 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 →
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