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FAM228B

Synonyms
-
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
9
Likely pathogenic
0
VUS
2,490
Likely benign
559
Benign
0

Patient Phenotypes

Proportions of phenotypes among 9 patients carrying pathogenic or likely pathogenic variants on FAM228B gene are displayed below. The following symptoms were found in patients with a variant in FAM228B. However, patients may have been diagnosed with a different variant.

Phenotype class
Patients in 3billion (%)
Abnormality of head or neck
33.3%
Abnormality of the nervous system
33.3%
Abnormality of limbs
22.2%
Abnormality of the eye
22.2%
Abnormality of the immune system
22.2%
Abnormality of the musculoskeletal system
22.2%
Growth abnormality
22.2%
Abnormality of blood and blood forming tissues
11.1%
Abnormality of metabolism homeostasis
11.1%
Abnormality of the ear
11.1%
Abnormality of the endocrine system
11.1%
Abnormality of the genitourinary system
11.1%
Abnormality of the integument
11.1%
Neoplasm
11.1%
Abnormal cellular phenotype
0%
Abnormality of prenatal development or birth
0%
Abnormality of the breast
0%
Abnormality of the cardiovascular system
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%

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