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Hi all, i have a genomic variant C.NM_000137.2:c.1021C>T, and i wanted to know how to where in literature it states it's pathogenic. For e.g. this link: http://www.jbc.org/content/276/18/15225.long talks about all the FAH variants but how do i know where this variation is stated pathogenic.
Thanks in advance
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You could have a look whether your variant is described as pathogenic in https://www.ncbi.nlm.nih.gov/clinvar/