SNX30-DT

Chr 9

SNX30 divergent transcript

0
Active trials
15
Pathogenic / LP
17
ClinVar variants
2
Pubs (1 yr)
Missense Z
LOEUF
Clinical SummarySNX30-DT
📋
ClinVar Variants
15 Pathogenic / Likely Pathogenic of 17 total submissions

Population Genetics & Constraint

Constraint data not available from gnomAD.

ClinVar Variant Classifications

17 submitted variants in ClinVar

Classification Summary

Pathogenic15
Likely Benign1
Benign1
15
Pathogenic
1
Likely Benign
1
Benign

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
15
Likely Pathogenic
0
VUS
0
Likely Benign
1
Benign
1
Total17

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

SNX30-DT · 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