TABLE 1.

Identification of all genetic variants included in the study.

Gene	dsSNP ID (rs)	SNP	Variant type	A.A residue	Context sequence [VIC/FAM]
ACTN3	rs1815739	R577X	Non-sense	R/STOP	CAAGGCAACACTGCCCGAGGCTGAC[T/C]GAGAGCGAGGTGCCATCATGGGCAT
VDR	rs2228570	FokI	Missense	K/R	GGAAGTGCTGGCCGCCATTGCCTCC[A/G]TCCCTGTAAGAACAGCAAGCAGGCC
VDR	rs731236	TaqI	Silent	I/I	TGGACAGGCGGTCCTGGATGGCCTC[A/G]ATCAGCGCGGCGTCCTGCACCCCAG
VDR	rs7975232	ApaI	Intron	–	AAGGCACAGGAGCTCTCAGCTGGGC[A/C]CCTCACTGCTCAATCCCACCACCCC

The bold values refers to the nucleotide change and the correspondence with the correspondent fluorocrome.