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CNIH1

Synonyms
CNIH, CNIH-1, CNIL, TGAM77
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
0
Likely pathogenic
0
VUS
529
Likely benign
6
Benign
0

Patient Phenotypes

No patients carry pathogenic or likely pathogenic variants on CNIH1 gene.

Phenotype class
Patients in 3billion (%)

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