rs1486835158
This variant is located in the ZNF778 gene.
▶ClinVar annotation
About ZNF778
The protein encoded by this gene is a member of the krueppel C2H2-type zinc-finger protein family, and it contains one KRAB domain and eighteen C2H2-type zinc fingers. This gene is a candidate gene for autism and variable cognitive impairment in the 16q24.3 microdeletion syndrome. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2011]
View all ZNF778 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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