Relative impact of indels versus SNPs on complex disease

AbstractIt is unclear whether insertions and deletions (indels) are more likely to influence complex traits than abundant single ‐nucleotide polymorphisms (SNPs). We sought to understand which category of variation is more likely to impact health. Using the SardiNIA study as an exemplar, we characterized 478,876 common indels and 8,246,244 common SNPs in up to 5,949 well‐phenotyped individuals from an isolated valley in S ardinia. We assessed association between 120 traits, resulting in 89 nonoverlapping‐associated loci.We evaluated whether indels were enriched among credible sets of potential causal variants. These credible sets included 1,319 SNPs and 88 indels. We did not find indels to be significantly enriched . Indels were the most likely causal variant in seven loci, including one locus associated with monocyte count where an indel with causality and mechanism previously demonstrated (rs200748895:TGCTG/T) had a 0.999 posterior probability. Overall, our results show a very modest and nonsignificant enric hment for common indels in associated loci.

Source: Genetic Epidemiology - November 22, 2018 Category: Epidemiology Authors: Sarah A. Gagliano, Sebanti Sengupta, Carlo Sidore, Andrea Maschio, Francesco Cucca, David Schlessinger, Gon çalo R. Abecasis Tags: BRIEF REPORT Source Type: research