rs200897838

This variant is located in the ABHD11 gene.

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ClinVar annotation

Uncertain Significance★☆☆☆

1 submitter

not specified

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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