SNHG4

Chr 5

small nucleolar RNA host gene 4

Also known as: NCRNA00059, U19H

33
ClinVar variants
15
Pathogenic / LP
pLI score
0
Active trials
Clinical SummarySNHG4
📋
ClinVar Variants
15 Pathogenic / Likely Pathogenic· 16 VUS of 33 total submissions
Some data sources returned errors (1)

gnomad: Error: Gene not found

Population Genetics & Constraint

Constraint data not available from gnomAD.

ClinVar Variant Classifications

33 submitted variants in ClinVar

Classification Summary

Pathogenic14
Likely Pathogenic1
VUS16
Likely Benign1
Benign1
14
Pathogenic
1
Likely Pathogenic
16
VUS
1
Likely Benign
1
Benign

Curated Variants Distribution

Classified variants from ClinVar · 5 ACMG categories

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
0
0
14
0
14
Likely Pathogenic
0
0
1
0
1
VUS
1
0
15
0
16
Likely Benign
0
0
1
0
1
Benign
0
0
1
0
1
Total1032033

LoF = frameshift, stop gained/lost, canonical splice · Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

SNHG4 · protein map & ClinVar variants

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

OMIM — Genotype-Phenotype Relationships

1 OMIM entry

Clinical Literature
Landmark / reviewRecent case evidence
Key Publications
Landmark & review papers · by relevance
PubMed
Top 10 resultsSearch PubMed ↗

Clinical Trials

Active and recruiting trials from ClinicalTrials.gov

No active trials found for this gene.

Search ClinicalTrials.gov →