FOLH1 — 75 ClinVar variants

All ClinVar germline FOLH1 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 57 flagged for review →

4 Benign · 9 Likely benign · 62 Uncertain significance

Full FOLH1 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 57

Variants where the independent computational evidence doesn't line up with the clinical picture — a QC signal for a second look, not a reclassification.

Predictors lean, ClinVar uncertain 51

ClinVar classifies these uncertain (VUS), but the independent predictors unanimously lean one way — a triage signal for review, not a reclassification.

All FOLH1 variants

Benign 4

Likely benign 9

Uncertain significance 62