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. 2020 Jul 3;57:102854. doi: 10.1016/j.ebiom.2020.102854

Table 1.

Circulating proteins with cis-pQTLs.

Protein Antibody P Top SNP Variant* TwinGene P§
CLEC3B HPA034794 5.31 × 10−38 rs4683026 Gly - Ser n.a.
HRG Bsi0137 3.65 × 10−25 rs12493926 Asn - Ile < 1 × 10−300
C1R HPA001551 2.18 × 10−22 rs1801046 Leu - Ser n.a.
GC Bsi0185 8.13 × 10−20 rs843005 Asp - Glu 1.17 × 10−95
CFH MAB4779 7.60 × 10−17 rs61818923 n.a.
CFH Bsi0885 1.81 × 10−16 rs1048663 Glu - Asp 8.96 × 10−269
AGT HPA001557 3.26 × 10−16 rs4762 Thr - Met n.a.
F9 HPA000254 5.16 × 10−16 rs422187 Thr - Ala n.a.
F12 Bsi0849 1.25 × 10−14 rs1801020 7.62 × 10−126
C4A OASA01015 5.15 × 10−14 rs386480 n.a.
LRG1 Bsi3134 8.50 × 10−10 rs10426311 n.a.
C6 Bsi0731 3.88 × 10−9 rs7443604 Ala - Glu 1.67 × 10−71
AHSG Bsi0907 4.58 × 10−9 rs13073106 Ser - Thr 1.24 × 10−16
FGL1 HPA049320 6.83 × 10−9 rs10093134 n.a.
HP Bsi1809 1.18 × 10−8 rs811053 4.86 × 10−88

The ID of the antibodies used in SBA assays.

Top associated SNP by ranking and the nominal P-value for the association (linear regression).

Non-synonymous SNPs in almost perfect linkage disequilibrium (LD) with the top SNP (R2 ≥ 0.8) in genomic data of Utah residents from north and West Europe (CEU) in the 1000 Genome project. The amino-acid variants were shown after the SNP ID. Additional details are provided in Table S6.

§

GWAS analysis conducted with the TwinGene cohort also revealed significant associations when matching SNPs with those identified in the S3WP study.