rs1574576373
This variant is located in the TMEM237 gene.
▶ClinVar annotation
Likely Benign★☆☆☆
1 submitter1 publicationAbout TMEM237
The protein encoded by this gene is a tetraspanin protein that is thought to be involved in WNT signaling. Defects in this gene are a cause of Joubert syndrome-14. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2012]
View all TMEM237 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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