. Author manuscript; available in PMC: 2013 Apr 1.

Published in final edited form as: Circ Cardiovasc Genet. 2012 Mar 14;5(2):234–241. doi: 10.1161/CIRCGENETICS.111.961763

Table 2.

Association between SNPs and carotid IMT at different anatomical sites

SNP	Gene	P values
SNP	Gene	BIF	CCA	ICA	Total
Chromosome 7
rs3815483	ANLN	0.00023	0.08852	0.11102	0.00360
rs2001600	AOAH	0.00092	0.02931	0.22562	0.00422
Chromosome 14
rs1667498	0	0.00679	0.04423	0.00627	0.00062
rs10144627	FOXN3	0.00131	0.00864	0.00088	0.00023
rs10151997	FOXN3	0.00160	0.00638	0.03823	0.00059
rs10151430	FOXN3	0.00547	0.02747	0.00764	0.00089
rs17803546	CCDC88C	0.02980	0.00369	0.00216	0.00056
rs7152362	PRIMA1	0.00262	0.00187	0.09807	0.00007

Each SNP was tested for association with maximum IMT at bifurcation (BIF), common carotid artery (CCA), internal carotid artery (ICA), and a mean composite measure of the IMT of all three carotid sites (Total). P values from the QTDT test in the 100 DR families are reported in the table.