SWINGN
Chr 13SWI/SNF complex interacting GAS6 enhancer non-coding RNA
Also known as: LINC00565
I cannot write a clinical gene summary for SWINGN because no information about this gene's protein function, associated diseases, or inheritance pattern has been provided in the data below the rules. To create an accurate clinical summary, I would need details about what protein this gene encodes, what conditions result from mutations, and the inheritance pattern observed in affected families.
Population Genetics & Constraint
Constraint data not available from gnomAD.
ClinVar Variant Classifications
130 submitted variants in ClinVar
Classification Summary
Curated Variants Distribution
Classified variants from ClinVar · 5 ACMG categories· variant type breakdown unavailable
| Classification | LoF | Missense + Inframe | Non-coding | Synonymous | Total |
|---|---|---|---|---|---|
Pathogenic | — | — | — | — | 112 |
Likely Pathogenic | — | — | — | — | 3 |
VUS | — | — | — | — | 13 |
Likely Benign | — | — | — | — | 1 |
Benign | — | — | — | — | 0 |
| Total | — | 129 | |||
Counts from ClinVar esearch · Updated hourly
View in ClinVar →Protein Context — Lollipop Plot
SWINGN · protein map & ClinVar variants
Showing all ClinVar variants across the protein. Search a specific variant to highlight its position.
External Resources
Links to major genomics databases and tools
Clinical Trials
Active and recruiting trials from ClinicalTrials.gov
No active trials found for this gene.
Search ClinicalTrials.gov →No open access results found
External Resources
Links to major genomics databases and tools