Table 2. Number of candidate variants filtered against dbSNP and 1000 Genomes public variation databases.

Single nucleotide variants (SNVs	Individuals
	II:3	II:1	I:1	I:2
Total SNVs	43,204	43,201	43,476	43,974
Non-synonymous SNVs	5850	5833	5888	5883
Filtered dbSNP	5752	5716	5781	5769
Filtered dbSNP and 1000 g	5697	5662	5735	5712
Filtered dbSNP and 1000 g and predicted deleterious	356	346	350	361