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SIDT2

Synonyms
CGI-40
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
19
Likely pathogenic
0
VUS
6,863
Likely benign
735
Benign
0

Patient phenotypes

Proportions of phenotypes among 19 patients carring pathogenic or likely pathogenic variants on SIDT2 gene are displayed below.

Phenotype class
Patients in 3billion (%)
Growth abnormality
52.6%
Abnormality of the musculoskeletal system
42.1%
Abnormality of the nervous system
31.6%
Abnormality of head or neck
26.3%
Abnormality of limbs
21.1%
Abnormality of the ear
15.8%
Abnormality of the eye
15.8%
Abnormality of blood and blood-forming tissues
10.5%
Abnormality of prenatal development or birth
10.5%
Abnormality of the cardiovascular system
10.5%
Abnormality of the digestive system
10.5%
Abnormality of the integument
10.5%
Abnormality of the endocrine system
5.3%
Abnormality of the genitourinary system
5.3%
Abnormality of the immune system
5.3%
Abnormality of the respiratory system
5.3%
Neoplasm
5.3%
Abnormal cellular phenotype
0%
Abnormality of metabolism homeostasis
0%
Abnormality of the breast
0%
Abnormality of the thoracic cavity
0%
Abnormality of the voice
0%
Constitutional symptom
0%

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