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R3HCC1L

Synonyms
C10orf28, GIDRP86, GIDRP88, PSORT
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
2,658
Likely benign
133
Benign
0

Patient phenotypes

No patients carry pathogenic or likely pathogenic variants on R3HCC1L gene.

Phenotype class
Patients in 3billion (%)

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