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VN1R4

Synonyms
V1RL4
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
1,921
Likely benign
124
Benign
0

Patient Phenotypes

Proportions of phenotypes among 21 patients carrying pathogenic or likely pathogenic variants on VN1R4 gene are displayed below. The following symptoms were found in patients with a variant in VN1R4. However, patients may have been diagnosed with a different variant.

Phenotype class
Patients in 3billion (%)
Abnormality of the nervous system
47.6%
Abnormality of the musculoskeletal system
38.1%
Abnormality of head or neck
33.3%
Abnormality of the eye
28.6%
Abnormality of the cardiovascular system
23.8%
Abnormality of the ear
14.3%
Growth abnormality
14.3%
Abnormality of the immune system
9.5%
Abnormality of the integument
9.5%
Abnormality of limbs
4.8%
Abnormality of metabolism homeostasis
4.8%
Abnormality of prenatal development or birth
4.8%
Abnormality of the digestive system
4.8%
Abnormality of the genitourinary system
4.8%
Abnormal cellular phenotype
0%
Abnormality of blood and blood forming tissues
0%
Abnormality of the breast
0%
Abnormality of the endocrine system
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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