SNHG18

Chr 5

small nucleolar RNA host gene 18

43
ClinVar variants
41
Pathogenic / LP
pLI score
0
Active trials
Clinical SummarySNHG18
📋
ClinVar Variants
41 Pathogenic / Likely Pathogenic of 43 total submissions

Population Genetics & Constraint

Constraint data not available from gnomAD.

ClinVar Variant Classifications

43 submitted variants in ClinVar

Classification Summary

Pathogenic41
Likely Benign2
41
Pathogenic
2
Likely Benign

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
41
Likely Pathogenic
0
VUS
0
Likely Benign
2
Benign
0
Total43

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

SNHG18 · protein map & ClinVar variants

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

OMIM — Genotype-Phenotype

No OMIM entries found.

Clinical Literature
Landmark / reviewRecent case evidence

Clinical Trials

Active and recruiting trials from ClinicalTrials.gov

No active trials found for this gene.

Search ClinicalTrials.gov →