SNHG7

Chr 9

small nucleolar RNA host gene 7

Also known as: NCRNA00061

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

0
Active trials
71
Pathogenic / LP
81
ClinVar variants
5
Pubs (1 yr)
Missense Z
LOEUF
Clinical SummarySNHG7
📋
ClinVar Variants
71 Pathogenic / Likely Pathogenic· 7 VUS of 81 total submissions

Population Genetics & Constraint

Constraint data not available from gnomAD.

ClinVar Variant Classifications

81 submitted variants in ClinVar

Classification Summary

Pathogenic68
Likely Pathogenic3
VUS7
Benign1
Conflicting2
68
Pathogenic
3
Likely Pathogenic
7
VUS
1
Benign
2
Conflicting

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
68
Likely Pathogenic
3
VUS
7
Likely Benign
0
Benign
1
Conflicting
2
Total81

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

SNHG7 · 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