Table 2.

Single nucleotide variants identified by re-sequencing chr14 QTL in Dominicans.

	Non-exonic	UTRs	Synonymous	NonSynonymous	Total
Rare Variant	3182 (61)*	411 (18)	132 (4)	144 (6)	3869
Common Variant	2029	240	86	76	2431
Total	5211	768	246	256	6300

*The number in parenthesis is the number of variants that are novel. Targeted re-sequencing of chr14 QTL was done in the Family study. Variants were categorized into different allele frequency categories based on imputation data generated from NOMAS. Variants with an estimated minor allele frequency greater than or equal to 5% in the NOMAS cohort are classified by common variant. Variants with an estimated minor allele frequency less than 5% or not imputed efficiently (INFO ≤ 0.4) in the NOMAS cohort are classified as rare variants.