rs782797932
This variant is located in the ABHD11 gene.
▶ClinVar annotation
About ABHD11
This gene encodes a protein containing an alpha/beta hydrolase fold domain. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. [provided by RefSeq, Mar 2016]
View all ABHD11 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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