rs91959
This variant is located in the APCDD1 gene.
▶ClinVar annotation
Benign★★★☆
2 submitters1 publicationAbout APCDD1
This locus encodes an inhibitor of the Wnt signaling pathway. Mutations at this locus have been associated with hereditary hypotrichosis simplex. Increased expression of this gene may also be associated with colorectal carcinogenesis.[provided by RefSeq, Sep 2010]
View all APCDD1 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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