Skip to main content
. Author manuscript; available in PMC: 2009 May 14.
Published in final edited form as: Nat Genet. 2008 Jan 13;40(2):189–197. doi: 10.1038/ng.75

Table 5. Genetic loci where common SNPs are associated with blood triglycerides.

Combined analysis: GWAS & ≤3 Replications GWAS: DGI Replication 1:
MDC-CC
Replication 2:
FINRISK97
Replication 3:
NORDIL
P P P P P
β β β β β
SNP Locus SNP type Nearest gene(s) Allele (frequency)a (s.e.m.)b (s.e.m.) (s.e.m.) (s.e.m.) (s.e.m.)
Newly identified loci
rs17145738 7q11 Intergenic BCL7B, TBL2,
MLXIPL
T (0.13) 7 × 10−22 0.003 3 × 10−8 2 × 10−7 3 × 10−7
−0.14 (0.02) −0.12 (0.04) −0.17 (0.03) −0.13 (0.02) −0.16 (0.03)
rs17321515 8q24 3′ downstream TRIB1 G (0.49) 4 × 10−17 7 × 10−4 1 × 10−5 7 × 10−5 8 × 10−7
−0.08 (0.01) −0.10 (0.03) −0.09 (0.02) −0.07 (0.02) −0.10 (0.02)
rs4846914 1q42 Intronic GALNT2 G (0.40) 7 × 10−15 9 × 10−5 0.001 2 × 10−8 0.01
0.08 (0.01) 0.11 (0.03) 0.07 (0.02) 0.09 (0.02) 0.05 (0.02)
rs16996148 19p13 Intergenic CILP2, PBX4 T (0.10) 4 × 10−9 0.05 0.23 2 × 10−5 3 × 10−5
−0.10 (0.02) −0.09 (0.05) −0.04 (0.03) −0.14 (0.03) −0.13 (0.03)
rs12130333 1p31 Intergenic ANGPTL3, DOCK7,
ATG4C
T (0.22) 2 × 10−8 0.0006 2 × 10−5 - -
−0.11 (0.02) −0.12 (0.03) −0.10 (0.02)
Loci with prior evidence
rs28927680c 11q23 5′ upstream APOA1-C3-A4-A5,
ZNF259, BUD13
G (0.07) 2 × 10−17 6 × 10−5 7 × 10−14 - -
0.26 (0.03) 0.22 (0.05) 0.29 (0.04)
rs693 2p24 Coding APOB A (0.48) 2 × 10−7 7 × 10−4 7 × 10−5 - -
0.08 (0.02) 0.09 (0.03) 0.08 (0.02)
rs780094d 2p23 Intronic GCKR T (0.34) 3 × 10−14 4 × 10−8 5 × 10−8 - -
0.13 (0.02) 0.16 (0.03) 0.11 (0.02)
rs328 8p21 Coding LPL G (0.09) 2 × 10−28 4 × 10−7e 9 × 10−9 2 × 10−10 2 × 10−6
−0.19 (0.02) −0.24 (0.05) −0.20 (0.03) −0.18 (0.03) −0.16 (0.03)

A dash (-) indicates that we did not genotype that SNP in sample. Beta-coefficient (β) represents the proportion of 1 s.d. change in standardized log triglycerides residual (mean = 0, s.d. = 1 after adjustment for age, age2, gender and diabetes status) per copy of the allele modeled.

a

Alleles for the SNP on the forward strand of human genome reference sequence (National Center for Biotechnology Information Build 35) were modeled. Allele frequency in the MDC-CC sample is presented.

b

Variance-weighted meta-analysis performed using data from up to four samples (DGI, MDC-CC, FINRISK and NORDIL), as described in Methods.

c

rs28927680 is highly correlated with APOA1-APOC3-APOA4-APOA5 coding SNP rs3133506 (r2 = 0.98 in MDC-CC); SNP rs3133506 (also known as 56C>G) has been reproducibly related to triglyceride and HDL cholesterol concentrations.

d

Data in this row on GCKR has been previously published6 and is presented here for completeness.

e

Association data from imputed SNP genotypes.