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OLFM3

Synonyms
NOE3, NOELIN3, OPTIMEDIN
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
32
Likely pathogenic
0
VUS
1,991
Likely benign
167
Benign
0

Patient phenotypes

Proportions of phenotypes among 32 patients carring pathogenic or likely pathogenic variants on OLFM3 gene are displayed below.

Phenotype class
Patients in 3billion (%)
Abnormality of the nervous system
28.1%
Abnormality of the cardiovascular system
21.9%
Abnormality of the musculoskeletal system
21.9%
Abnormality of the ear
18.8%
Abnormality of head or neck
12.5%
Abnormality of the digestive system
9.4%
Growth abnormality
9.4%
Abnormality of the genitourinary system
6.3%
Abnormality of blood and blood-forming tissues
3.1%
Abnormality of limbs
3.1%
Abnormality of prenatal development or birth
3.1%
Abnormality of the eye
3.1%
Abnormal cellular phenotype
0%
Abnormality of metabolism homeostasis
0%
Abnormality of the breast
0%
Abnormality of the endocrine system
0%
Abnormality of the immune system
0%
Abnormality of the integument
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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