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MYRIP

Synonyms
SLAC2-C, SLAC2C
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
3,470
Likely benign
545
Benign
0

Patient phenotypes

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

Phenotype class
Patients in 3billion (%)

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