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C16orf78

Synonyms
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External resources
Summary
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Variant counts

The variants found in rare patients tested by 3billion are classified and counted according to ACMG guidelines. The variants with over 5% variant frequency in population genome databases ( gnomAD, dbSNP, etc) are excluded.

Pathogenic
0
Likely pathogenic
0
VUS
1,007
Likely benign
1,356
Benign
0

Patient phenotypes

No patients carry pathogenic or likely pathogenic variants on C16orf78 gene.

Phenotype class
Patients in 3billion (%)

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