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ODF2L

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
21
Likely pathogenic
0
VUS
6,981
Likely benign
183
Benign
0

Patient phenotypes

Proportions of phenotypes among 21 patients carring pathogenic or likely pathogenic variants on ODF2L gene are displayed below.

Phenotype class
Patients in 3billion (%)
Abnormality of the nervous system
47.6%
Abnormality of head or neck
28.6%
Abnormality of the digestive system
23.8%
Abnormality of the ear
23.8%
Abnormality of the integument
23.8%
Abnormality of the musculoskeletal system
23.8%
Abnormality of the eye
19%
Abnormality of limbs
14.3%
Abnormality of the cardiovascular system
14.3%
Abnormality of the genitourinary system
14.3%
Abnormality of the respiratory system
14.3%
Growth abnormality
14.3%
Abnormality of prenatal development or birth
9.5%
Abnormality of the immune system
9.5%
Constitutional symptom
4.8%
Abnormal cellular phenotype
0%
Abnormality of blood and blood-forming tissues
0%
Abnormality of metabolism homeostasis
0%
Abnormality of the breast
0%
Abnormality of the endocrine system
0%
Abnormality of the thoracic cavity
0%
Abnormality of the voice
0%
Neoplasm
0%

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