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VN1R5

Synonyms
V1RL5
External resources
Summary
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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
4
Likely pathogenic
0
VUS
458
Likely benign
0
Benign
0

Patient Phenotypes

Proportions of phenotypes among 4 patients carrying pathogenic or likely pathogenic variants on VN1R5 gene are displayed below. The following symptoms were found in patients with a variant in VN1R5. However, patients may have been diagnosed with a different variant.

Phenotype class
Patients in 3billion (%)
Abnormality of the eye
75%
Abnormality of the integument
75%
Abnormality of the musculoskeletal system
75%
Abnormality of limbs
50%
Growth abnormality
50%
Abnormality of blood and blood forming tissues
25%
Abnormality of head or neck
25%
Abnormality of metabolism homeostasis
25%
Abnormality of the cardiovascular system
25%
Abnormality of the ear
25%
Abnormality of the nervous system
25%
Abnormal cellular phenotype
0%
Abnormality of prenatal development or birth
0%
Abnormality of the breast
0%
Abnormality of the digestive system
0%
Abnormality of the endocrine system
0%
Abnormality of the genitourinary system
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%
Neoplasm
0%

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