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MKRN2OS

Synonyms
C3orf83, MKRN2-AS1
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
903
Likely benign
1,097
Benign
0

Patient phenotypes

Proportions of phenotypes among 19 patients carring pathogenic or likely pathogenic variants on MKRN2OS gene are displayed below.

Phenotype class
Patients in 3billion (%)
Abnormality of the nervous system
47.4%
Abnormality of the eye
36.8%
Abnormality of head or neck
31.6%
Abnormality of the musculoskeletal system
26.3%
Abnormality of the cardiovascular system
21.1%
Growth abnormality
21.1%
Abnormality of the integument
15.8%
Abnormality of limbs
10.5%
Abnormality of the genitourinary system
10.5%
Abnormality of blood and blood-forming tissues
5.3%
Abnormality of prenatal development or birth
5.3%
Abnormality of the ear
5.3%
Abnormality of the endocrine system
5.3%
Abnormality of the immune system
5.3%
Abnormal cellular phenotype
0%
Abnormality of metabolism homeostasis
0%
Abnormality of the breast
0%
Abnormality of the digestive 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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