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IFNA13

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
35
Likely pathogenic
0
VUS
554
Likely benign
342
Benign
0

Patient Phenotypes

Proportions of phenotypes among 35 patients carrying pathogenic or likely pathogenic variants on IFNA13 gene are displayed below. The following symptoms were found in patients with a variant in IFNA13. However, patients may have been diagnosed with a different variant.

Phenotype class
Patients in 3billion (%)
Abnormality of the nervous system
34.3%
Abnormality of the musculoskeletal system
22.9%
Abnormality of head or neck
20%
Abnormality of the cardiovascular system
20%
Abnormality of the ear
14.3%
Abnormality of metabolism homeostasis
11.4%
Growth abnormality
11.4%
Abnormality of blood and blood forming tissues
8.6%
Abnormality of the endocrine system
5.7%
Abnormality of the eye
5.7%
Abnormality of the integument
5.7%
Neoplasm
5.7%
Abnormality of limbs
2.9%
Abnormality of the breast
2.9%
Abnormality of the digestive system
2.9%
Abnormality of the genitourinary system
2.9%
Abnormal cellular phenotype
0%
Abnormality of prenatal development or birth
0%
Abnormality of the immune 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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