rs1459825302

This variant is located in the DIS3L2 gene.

ClinVar annotation

Likely Benign☆☆☆
1 submitter1 publication

Perlman syndrome

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About DIS3L2

The protein encoded by this gene is similar in sequence to 3'/5' exonucleolytic subunits of the RNA exosome. The exosome is a large multimeric ribonucleotide complex responsible for degrading various RNA substrates. Several transcript variants, some protein-coding and some not, have been found for this gene. [provided by RefSeq, Mar 2012]

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Gene information from NCBI Gene. Variant classifications from ClinVar.

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