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C6

complement C6

HCNC Approved Symbol
C6 (HGNC:1339)
Genomic Coordinates
5:41,142,116 - 41,261,469 (5p13.1)
Synonyms
Disease Associations
This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

2Patients

In total, 2 patients were diagnosed with a variant in the C6 gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

Eversion of lateral third of lower eyelids
 1 (50.0%)
Facial dysmorphism
 1 (50.0%)
Failure to thrive
 1 (50.0%)
Global developmental delay
 1 (50.0%)
High arched palate
 1 (50.0%)
C6 - Gene browser | 3billion