FAM242F
Chr 9family with sequence similarity 242 member F
Clinical Summary— FAM242F
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ClinVar Variants
19 Pathogenic / Likely Pathogenic of 19 total submissions
Some data sources returned errors (2)
gnomad: Error: Gene not found
pubtator: Error: PubTator3 HTTP 502
Population Genetics & Constraint
Constraint data not available from gnomAD.
ClinVar Variant Classifications
19 submitted variants in ClinVar
Classification Summary
Pathogenic18
Likely Pathogenic1
18
Pathogenic
1
Likely Pathogenic
Curated Variants Distribution
Classified variants from ClinVar · 5 ACMG categories· variant type breakdown unavailable
| Classification | LoF | Missense + Inframe | Non-coding | Synonymous | Total |
|---|---|---|---|---|---|
Pathogenic | — | — | — | — | 18 |
Likely Pathogenic | — | — | — | — | 1 |
VUS | — | — | — | — | 0 |
Likely Benign | — | — | — | — | 0 |
Benign | — | — | — | — | 0 |
| Total | — | 19 | |||
Counts from ClinVar esearch · Updated hourly
View in ClinVar →FAM242F · 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 →Clinical Literature
Landmark / reviewRecent case evidence
No publications found for FAM242F
External Resources
Links to major genomics databases and tools