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MAGIX

Synonyms
JM10, PDZX
External resources

Variant Counts

Variant classification counts, according to ACMG guideline on all identified variants among our tested samples, are listed. The variants with over 5% variant frequency in population genome databases ( gnomAD, dbSNP, etc.) are excluded.

Pathogenic
22
Likely pathogenic
3
VUS
2,115
Likely benign
1
Benign
0

Patient Phenotypes

Proportions of phenotypes among 25 patients carrying pathogenic or likely pathogenic variants on MAGIX gene are displayed below. The following symptoms were found in patients with a variant in MAGIX. However, patients may have been diagnosed with a different variant.

Phenotype class
Patients in 3billion (%)
Abnormality of the nervous system
44%
Abnormality of the musculoskeletal system
36%
Abnormality of head or neck
20%
Abnormality of limbs
16%
Abnormality of the eye
12%
Abnormality of the cardiovascular system
8%
Abnormality of the digestive system
8%
Abnormality of the ear
8%
Abnormality of the integument
8%
Growth abnormality
8%
Abnormality of blood and blood forming tissues
4%
Abnormality of metabolism homeostasis
4%
Abnormality of the immune system
4%
Neoplasm
4%
Abnormal cellular phenotype
0%
Abnormality of prenatal development or birth
0%
Abnormality of the breast
0%
Abnormality of the endocrine system
0%
Abnormality of the genitourinary system
0%
Abnormality of the respiratory system
0%
Abnormality of the thoracic cavity
0%
Abnormality of the voice
0%
Constitutional symptom
0%

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