Is DMD c.(?_32 pathogenic?

DMD c.(?32 is classified Pathogenic in DMD (ClinVar, Single submitter, 1 submitter; last evaluated 2016-08-19). Associated with muscular dystrophy.

What condition is associated with DMD c.(?_32?

DMD c.(?_32 is associated with muscular dystrophy (ClinVar).

DMD c.(?_32

VCV505317

Pathogenic Single submitter

Classification

Pathogenic

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

gnomAD v4.1

Rare

Conditions

muscular dystrophy

Computational evidence

Protein change
Missense predictors do not apply to this variant type.

Variant & gene context

Gene: DMD
Coding: c.(?_32
MANE Select: NM_004006
Type: Deletion
Location: chrX:None (GRCh38)

Full DMD gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

muscular dystrophy — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Similar variants

DMD p.Thr1683fs Pathogenic ★ same condition
DMD p.Leu1424Ter Pathogenic/Likely pathogenic ★★ same condition
DMD p.Arg2524His Benign/Likely benign ★★ same condition
DMD c.357+1G>A Likely pathogenic ★ same condition
DMD c.1812+601A>G Uncertain significance ★ same condition
DMD c.9225-1G>C Uncertain significance ★ same condition
DMD p.Leu575Pro Conflicting classifications of pathogenicity ★ ⚠ same condition
DMD c.1150-14_1158dup Pathogenic same condition

Built on 18 open, versioned datasets — ClinVar, gnomAD, AlphaMissense, REVEL, ClinGen & more — plus Sugi Variant's own cross-source analysis. Source data 2026-01–2026-10, ClinVar 2026-10. Full sources & versions →

Cite Sugi Variant

Gür T. Sugi Variant: A Deterministic Per-Variant Germline Reference from a Knowledge Graph for Humans and AI Agents. 2026. doi:10.5281/zenodo.21509445. This variant: https://sugi.bio/variant/dmd-c-32 (accessed [today's date]).

Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown