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. Author manuscript; available in PMC: 2020 Dec 11.
Published in final edited form as: Br J Haematol. 2020 Mar 30;190(5):783–786. doi: 10.1111/bjh.16613

Table 1. The association of any VTE or recurrent VTE with genotypes for F5, FAM134B, MYH8, and two MYH variant sets containing either 7 or 9 MYH SNPs.

The association of F5 rs6025, FAM134B rs78314670, MYH8 rs111567318, and two variant sets of MYH variants were made for all VTE cases (N=104) vs controls (N=211) and for adult recurrent VTE cases (N=32) vs. controls (N=211), as noted. See Table 4S listing for 7 rare MYH variants with MAF < 0.01 and 2 uncommon MYH variants with MAF > 0.01 and < 0.05 which were used to define sets of MYH variants that were collapsed into the two variant sets used for comparisons in this Table.

Gene SNP MAF p value
control (N=211) VTE all cases (N=104) VTE recurrence (N=32) VTE all cases VTE recurrence
F5 rs6025 0.021 0.130 0.141 3.46 x 10−8 2.68 x 10−6
FAM134B rs78314670 0.002 0.037 0.078 3.10 x 10−4 3.37 x 10−7
MYH8 rs111567318 0 0.019 0.047 4.10 x 10−3 8.55 x 10−6
MYH variant set 7 rare SNPs (MYH1,2,8) 0 0.063 0.156 2.11 x 10−7 2.70 x 10−16
MYH variant set 7 rare + 2 uncommon SNPs (MYH1,2,4,8) 0.047 0.125 0.219 4.30 x 10−4 6.03 x 10−7