FAM90A11
Chr 8family with sequence similarity 90 member A11
Also known as: FAM90A11P
Clinical Summary— FAM90A11
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ClinVar Variants
35 Pathogenic / Likely Pathogenic of 94 total submissions
Population Genetics & Constraint
Constraint data not available from gnomAD.
ClinVar Variant Classifications
94 submitted variants in ClinVar
Classification Summary
Pathogenic35
Benign58
Conflicting1
35
Pathogenic
58
Benign
1
Conflicting
Curated Variants Distribution
Classified variants from ClinVar · 5 ACMG categories· variant type breakdown unavailable
| Classification | LoF | Missense + Inframe | Non-coding | Synonymous | Total |
|---|---|---|---|---|---|
Pathogenic | — | — | — | — | 35 |
Likely Pathogenic | — | — | — | — | 0 |
VUS | — | — | — | — | 0 |
Likely Benign | — | — | — | — | 0 |
Benign | — | — | — | — | 58 |
Conflicting | — | 1 | |||
| Total | — | 94 | |||
Counts from ClinVar esearch · Updated hourly
View in ClinVar →FAM90A11 · 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 FAM90A11
External Resources
Links to major genomics databases and tools