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TMEM59L

Synonyms
BSMAP, C19orf4
External resources
Summary
This gene encodes a predicted type-I membrane glycoprotein. The encoded protein may play a role in functioning of the central nervous system.

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
816
Likely benign
1,262
Benign
0

Patient phenotypes

No patients carry pathogenic or likely pathogenic variants on TMEM59L gene.

Phenotype class
Patients in 3billion (%)

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