SNORA38B

Chr 17

small nucleolar RNA, H/ACA box 38B

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

0
Active trials
3
Pathogenic / LP
3
ClinVar variants
0
Pubs (1 yr)
Missense Z
LOEUF
Clinical SummarySNORA38B
📋
ClinVar Variants
3 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

SNORA38B · protein map & ClinVar variants

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

Clinical Trials

Active and recruiting trials from ClinicalTrials.gov

No active trials found for this gene.

Search ClinicalTrials.gov →
Clinical Literature
Landmark / reviewRecent case evidence