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C2orf74

Synonyms
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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
10
Likely pathogenic
0
VUS
395
Likely benign
19
Benign
0

Patient Phenotypes

Proportions of phenotypes among 10 patients carrying pathogenic or likely pathogenic variants on C2orf74 gene are displayed below. The following symptoms were found in patients with a variant in C2orf74. However, patients may have been diagnosed with a different variant.

Phenotype class
Patients in 3billion (%)
Abnormality of the eye
30%
Abnormality of the musculoskeletal system
30%
Abnormality of the nervous system
30%
Abnormality of head or neck
20%
Abnormality of metabolism homeostasis
20%
Abnormality of the cardiovascular system
20%
Growth abnormality
20%
Abnormal cellular phenotype
10%
Abnormality of blood and blood forming tissues
10%
Abnormality of limbs
10%
Abnormality of the digestive system
10%
Abnormality of the genitourinary system
10%
Abnormality of the immune system
10%
Abnormality of the integument
10%
Abnormality of the respiratory system
10%
Abnormality of the voice
10%
Abnormality of prenatal development or birth
0%
Abnormality of the breast
0%
Abnormality of the ear
0%
Abnormality of the endocrine system
0%
Abnormality of the thoracic cavity
0%
Constitutional symptom
0%
Neoplasm
0%

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