Germline sequence variants in TGM3 and RGS22 confer risk of basal cell carcinoma

Abstract

To search for new sequence variants that confer risk of cutaneous basal cell carcinoma (BCC), we conducted a genome-wide association study of 38.5 million single nucleotide polymorphisms (SNPs) and small indels identified through whole-genome sequencing of 2230 Icelanders. We imputed genotypes for 4208 BCC patients and 109 408 controls using Illumina SNP… (More)
DOI: 10.1093/hmg/ddt671

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