rs376353035
This variant is located in the AMER1 gene.
▶ClinVar annotation
Likely Benign★★★☆
2 submitters1 publicationAbout AMER1
The protein encoded by this gene upregulates trancriptional activation by the Wilms tumor protein and interacts with many other proteins, including CTNNB1, APC, AXIN1, and AXIN2. Defects in this gene are a cause of osteopathia striata with cranial sclerosis (OSCS). [provided by RefSeq, May 2010]
View all AMER1 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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