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CWF19L2

Synonyms
-
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
14
Likely pathogenic
0
VUS
15,068
Likely benign
1,501
Benign
0

Patient Phenotypes

Proportions of phenotypes among 14 patients carrying pathogenic or likely pathogenic variants on CWF19L2 gene are displayed below. The following symptoms were found in patients with a variant in CWF19L2. However, patients may have been diagnosed with a different variant.

Phenotype class
Patients in 3billion (%)
Abnormality of the musculoskeletal system
50%
Abnormality of the nervous system
42.9%
Abnormality of head or neck
28.6%
Abnormality of the eye
28.6%
Abnormality of limbs
21.4%
Abnormality of the cardiovascular system
14.3%
Abnormality of the digestive system
14.3%
Constitutional symptom
14.3%
Abnormality of metabolism homeostasis
7.1%
Abnormality of the ear
7.1%
Abnormality of the voice
7.1%
Abnormal cellular phenotype
0%
Abnormality of blood and blood forming tissues
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 immune system
0%
Abnormality of the integument
0%
Abnormality of the respiratory system
0%
Abnormality of the thoracic cavity
0%
Growth abnormality
0%
Neoplasm
0%

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