Table 1.
SNP ID | Allele1 | Allele2 | Effect Allele | Effect Allele Frequency | Location on Chr 7 | B | SE | P Value |
---|---|---|---|---|---|---|---|---|
rs12706544 | A | C | C | 0.23 | 123092680 | −0.032 | 0.013 | 0.014 |
rs1019219 | T | C | C | 0.08 | 123106873 | −0.014 | 0.020 | 0.497 |
rs1073682 | G | C | C | 0.99 | 123110320 | −0.019 | 0.061 | 0.753 |
rs6971373 | A | G | G | 0.01 | 123121498 | 0.016 | 0.063 | 0.795 |
rs6975039 | T | C | C | 0.93 | 123134504 | −0.015 | 0.022 | 0.486 |
rs12706551 | T | G | G | 0.96 | 123166013 | 0.059 | 0.031 | 0.060 |
rs2069269 | G | C | C | 0.92 | 123193642 | −0.022 | 0.020 | 0.280 |
rs623201 | T | C | C | 0.23 | 123194511 | −0.014 | 0.013 | 0.299 |
rs600420 | A | G | G | 0.60 | 123195286 | −0.031 | 0.011 | 0.005 |
Carotid‐femoral pulse wave velocity was inverted and standardized before analysis. B indicates difference in standardized inverse carotid‐femoral pulse wave velocity per dose of the coded allele; Chr, chromosome; SNP, single nucleotide polymorphism.