VMA21 Chromosome X
Vacuolar ATPase assembly factor VMA21
Upload your DNA to see your personal genotypes for variants in VMA21.
What This Gene Does
This gene encodes a chaperone for assembly of lysosomal vacuolar ATPase.[provided by RefSeq, Jul 2012]
Associated Conditions (3)
X-linked myopathy with excessive autophagy
Inborn genetic diseases
VMA21-related disorder
Key Variants
RS143565725
Conflicting classifications of pathogenicity
X-linked myopathy with excessive autophagy, Inborn genetic diseases, X-linked myopathy with excessive autophagy
Health Risk
RS1465930949
Conflicting classifications of pathogenicity
X-linked myopathy with excessive autophagy, Inborn genetic diseases, X-linked myopathy with excessive autophagy
Health Risk
RS765120199
Conflicting classifications of pathogenicity
X-linked myopathy with excessive autophagy, Inborn genetic diseases, VMA21-related disorder
Health Risk
RS878854355
Conflicting classifications of pathogenicity
X-linked myopathy with excessive autophagy, X-linked myopathy with excessive autophagy
Health Risk
RS878854354
Likely pathogenic
X-linked myopathy with excessive autophagy, X-linked myopathy with excessive autophagy
Health Risk
RS1556035617
Pathogenic
X-linked myopathy with excessive autophagy, X-linked myopathy with excessive autophagy
Health Risk
RS797044909
Pathogenic
X-linked myopathy with excessive autophagy, Inborn genetic diseases, X-linked myopathy with excessive autophagy
Health Risk
RS878854352
Pathogenic
X-linked myopathy with excessive autophagy, X-linked myopathy with excessive autophagy, X-linked myopathy with excessive autophagy
Health Risk
RS878854353
Pathogenic
X-linked myopathy with excessive autophagy, X-linked myopathy with excessive autophagy
Health Risk
RS878854356
Pathogenic
X-linked myopathy with excessive autophagy, X-linked myopathy with excessive autophagy
Health Risk
RS878854357
Pathogenic
X-linked myopathy with excessive autophagy, X-linked myopathy with excessive autophagy
Health Risk
All Variants (11)
| RSID | Category | Clinical Significance | Conditions |
|---|---|---|---|
| RS143565725 | Health Risk | Conflicting classifications of pathogenicity | X-linked myopathy with excessive autophagy, Inborn genetic diseases, X-linked myopathy with excessive autophagy |
| RS1465930949 | Health Risk | Conflicting classifications of pathogenicity | X-linked myopathy with excessive autophagy, Inborn genetic diseases, X-linked myopathy with excessive autophagy |
| RS765120199 | Health Risk | Conflicting classifications of pathogenicity | X-linked myopathy with excessive autophagy, Inborn genetic diseases, VMA21-related disorder |
| RS878854355 | Health Risk | Conflicting classifications of pathogenicity | X-linked myopathy with excessive autophagy, X-linked myopathy with excessive autophagy |
| RS878854354 | Health Risk | Likely pathogenic | X-linked myopathy with excessive autophagy, X-linked myopathy with excessive autophagy |
| RS1556035617 | Health Risk | Pathogenic | X-linked myopathy with excessive autophagy, X-linked myopathy with excessive autophagy |
| RS797044909 | Health Risk | Pathogenic | X-linked myopathy with excessive autophagy, Inborn genetic diseases, X-linked myopathy with excessive autophagy |
| RS878854352 | Health Risk | Pathogenic | X-linked myopathy with excessive autophagy, X-linked myopathy with excessive autophagy, X-linked myopathy with excessive autophagy |
| RS878854353 | Health Risk | Pathogenic | X-linked myopathy with excessive autophagy, X-linked myopathy with excessive autophagy |
| RS878854356 | Health Risk | Pathogenic | X-linked myopathy with excessive autophagy, X-linked myopathy with excessive autophagy |
| RS878854357 | Health Risk | Pathogenic | X-linked myopathy with excessive autophagy, X-linked myopathy with excessive autophagy |