FAM41AY2
Chr Yfamily with sequence similarity 41 member A, Y-linked 2
I cannot provide a clinical summary for FAM41AY2 as no information about this gene's protein function, associated diseases, or inheritance pattern was provided in the data below the instructions. A complete clinical summary requires information about what the protein does, what conditions result from mutations, and the inheritance pattern.
Population Genetics & Constraint
Constraint data not available from gnomAD.
ClinVar Variant Classifications
34 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 | — | — | — | — | 24 |
Likely Pathogenic | — | — | — | — | 2 |
VUS | — | — | — | — | 3 |
Likely Benign | — | — | — | — | 4 |
Benign | — | — | — | — | 0 |
Conflicting | — | 1 | |||
| Total | — | 34 | |||
Counts from ClinVar esearch · Updated hourly
View in ClinVar →Protein Context — Lollipop Plot
FAM41AY2 · protein map & ClinVar variants
Showing all ClinVar variants across the protein. Search a specific variant to highlight its position.
3D Protein StructureAlphaFold
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