SNORA84

Chr 9

small nucleolar RNA, H/ACA box 84

SNORA84 encodes a small nucleolar RNA predicted to be involved in RNA processing within the nucleolus. Currently, no established human diseases have been definitively associated with mutations in this gene, and the inheritance pattern remains undetermined. Further clinical and molecular studies are needed to establish any disease associations.

ResearchSummary from RefSeq
Clinical SummarySNORA84
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ClinVar Variants
13 unique Pathogenic / Likely Pathogenic· 2 VUS of 15 total submissions

Population Genetics & Constraint

Constraint data not available from gnomAD.

ClinVar Variant Classifications

15 submitted variants in ClinVar

Classification Summary

Pathogenic13
VUS2
13
Pathogenic
2
VUS

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
13
Likely Pathogenic
0
VUS
2
Likely Benign
0
Benign
0
Total15

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

SNORA84 · 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.

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Clinical Literature
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Recent Gene-Specific Literature
Gene in title · MEDLINE · newest first
Europe PMC

No open access results found