Table 1. Effect estimates for plasma phospholipid levels of polyunsaturated fatty acids (PUFAs, % of total fatty acids) for genome-wide significant (P<5 × 10−8), independent (r 2 <0.1) genetic variants reported from previous GWAS.
Chr | SNP | GRCh37/hg19 position | Allelea | EAF | β | s.e. | P-value | % VEb per allele | % VE per IVc | F-statistic per IVd |
---|---|---|---|---|---|---|---|---|---|---|
Linoleic acid (LA, 18:2n6) | ||||||||||
10 | rs10740118 | 65101207 | C/G | 0.56 | 0.248 | 0.043 | 8.08 × 10−9 | 0.2–0.7 | ||
11 | rs174547 | 61570783 | T/C | 0.32 | 1.474 | 0.042 | 4.98 × 10−274 | 7.6–18.1 | ||
11 | rs2727270 | 61603237 | T/C | 0.44 | 0.690 | 0.070 | 2.60 × 10−21 | 0.5–2.4 | ||
16 | rs16966952 | 15135943 | A/G | 0.31 | 0.351 | 0.044 | 1.23 × 10−15 | 0.5–2.5 | 8.8–23.6e | 1104–3533 |
Arachidonic acid (AA, 20:4n6) | ||||||||||
11 | rs174547 | 61570783 | T/C | 0.68 | 1.691 | 0.025 | 3.00 × 10−971 | 32.63 | ||
16 | rs16966952 | 15135943 | A/G | 0.69 | 0.199 | 0.031 | 2.43 × 10−10 | 0.44 | 33.07 | 11 302 |
α-Linolenic acid (ALA, 18:3n3) | ||||||||||
11 | rs174547 | 61570783 | T/C | 0.33 | 0.016 | 0.001 | 3.47 × 10−64 | 1.03 | 1.03 | 476 |
Eicosapentaenoic acid (EPA, 20:5n3) | ||||||||||
6 | rs3798713 | 11008622 | C/G | 0.43 | 0.035 | 0.005 | 1.93 × 10−12 | 0.36 | ||
11 | rs174538 | 61560081 | A/G | 0.72 | 0.083 | 0.005 | 5.37 × 10−58 | 1.69 | 2.05 | 479 |
Docosapentaenoic acid (DPA, 22:5n3) | ||||||||||
2 | rs780094 | 27741237 | T/C | 0.41 | 0.017 | 0.003 | 9.04 × 10−09 | 0.46 | ||
6 | rs3734398 | 10982973 | T/C | 0.43 | 0.040 | 0.003 | 9.61 × 10−44 | 2.74 | ||
11 | rs174547 | 61570783 | T/C | 0.67 | 0.075 | 0.003 | 3.79 × 10−154 | 8.38 | 11.58 | 1997 |
Docosahexaenoic acid (DHA, 22:6n3) | ||||||||||
6 | rs2236212 | 10995015 | C/G | 0.57 | 0.113 | 0.014 | 1.26 × 10−15 | 0.65 | 0.65 | 299 |
Abbreviations: EAF=effect allele frequency; IV=instrumental variable; s.e.=standard error; SNP=single-nucleotide polymorphism.
Allele associated with an increase in PUFA levels is in bold, and is considered the effect allele.
% variation explained (VE)=(2 × β2 × EAF × (1−EAF)/var(PUFA)) × 100.
% VE per IV=sum of the %VE per allele for each SNP included in the IV.
F-statistic is a measure of the strength of the genetic instrument and is calculated as follows: (R2 × (n-1-k))/((1-R2) × k), where R2=% variation explained, n= sample size, k=total number of instrumental variables.
Ranges for % VE per SNP and % VE IV as reported in Guan et al (2014).