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VSIG2

Synonyms
2210413P10Rik, CTH, CTXL
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
24
Likely pathogenic
0
VUS
12,145
Likely benign
968
Benign
0

Patient Phenotypes

Proportions of phenotypes among 24 patients carrying pathogenic or likely pathogenic variants on VSIG2 gene are displayed below. The following symptoms were found in patients with a variant in VSIG2. However, patients may have been diagnosed with a different variant.

Phenotype class
Patients in 3billion (%)
Abnormality of the musculoskeletal system
33.3%
Abnormality of the nervous system
33.3%
Abnormality of the cardiovascular system
20.8%
Abnormality of the eye
20.8%
Abnormality of limbs
12.5%
Abnormality of the genitourinary system
12.5%
Abnormality of head or neck
8.3%
Abnormality of the ear
8.3%
Abnormality of the integument
8.3%
Abnormality of blood and blood forming tissues
4.2%
Abnormality of metabolism homeostasis
4.2%
Abnormality of prenatal development or birth
4.2%
Abnormality of the breast
4.2%
Abnormality of the digestive system
4.2%
Abnormality of the endocrine system
4.2%
Abnormality of the immune system
4.2%
Growth abnormality
4.2%
Abnormal cellular phenotype
0%
Abnormality of the respiratory system
0%
Abnormality of the thoracic cavity
0%
Abnormality of the voice
0%
Constitutional symptom
0%
Neoplasm
0%

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