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. Author manuscript; available in PMC: 2020 Oct 1.
Published in final edited form as: Cancer Epidemiol Biomarkers Prev. 2020 Feb 12;29(4):860–870. doi: 10.1158/1055-9965.EPI-19-0891

Table 1.

Single nucleotide polymorphisms (SNPs) identified from published genome-wide association studies (GWAS) used to construct genetic instruments for polyunsaturated fatty acids (PUFA)

Polyunsaturated fatty acids (chain length) Number of SNPs used in instrument % variation Explaineda 1 SD Increase in wGSb (%) Independent SNPs included in instrumentc
Omega-6
 Linoleic acid (LA; 18:2) 4 8.8 – 23.6 1.18 rs10740118, rs174547, rs2727270, rs16966952
 Arachidonic acid (AA; 20:2) 2 33.1 1.11 rs174547, rs16966952
Omega-3
 α-linolenic acid (ALA; 18:3) 1 1.0 0.01 rs174547
 Eicosapentaenoic acid (EPA; 20:5) 2 2.1 0.06 rs3798713, rs174538
 Docosapentaenoic acid (DPA; 22:5) 3 11.6 0.06 rs780094, rs3734398, rs174547
 Docosahexaenoic acid (DHA; 22:6) 1 0.7 0.08 rs2236212
a

Percent variation explained per instrument calculated as follows: in[2βi2MAF(1-MAF)/variance(PUFA)]*100, where n is the number of independent SNPs, β is effect estimate from GWAS, MAF is the minor allele frequency, and variance is PUFA-specific.[22]

b

Each PUFA-specific weighted-genetic score (wGS) represents a genetically-predicted level of PUFAs, which represent an increase in total percent of plasma fatty acids. Weights used to create the wGS were obtained from previous genome-wide association studies (GWAS).[20,21]

c

SNPs used in each instrument are independent with linkage disequilibrium (LD; as measured using the correlation coefficient, r2) less than 0.1.