SLC16A7 — 74 ClinVar variants

All ClinVar germline SLC16A7 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 64 flagged for review →

2 Benign · 4 Likely benign · 68 Uncertain significance

Full SLC16A7 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 64

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 SLC16A7 variants

Benign 2

Likely benign 4

Uncertain significance 68