|| common in complete genomics
|?|| (C;C) (C;T) (T;T) ||28|
] A genome-wide survey of the prevalence and evolutionary forces acting on human nonsense SNPs.
[PMID 19420133] Characterization of sulfoxygenation and structural implications of human flavin-containing monooxygenase isoform 2 (FMO2.1) variants S195L and N413K.
[PMID 21205862] Gene inactivation and its implications for annotation in the era of personal genomics.
|| not reviewed
|| Insufficiently evaluated not reviewed