Table 2.

List of the different types and localizations of the 151 identified “in common variations”

Identified SNPs	N = 151
Missense Variants	93
Synonymous Variants	19
Stop Gained Variant	1
Frameshift Variants	2
Inframe Deletion	1
Splice Acceptor Variants	2
Intron Variants	7
3 Prime UTR Variants	13
5 Prime UTR Variants	2
Non Coding Transcript Variants	8
upstream_gene_variants	3

SNP: single nucleotide polymorphisms N: number of variants UTR: untranslated region