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. Author manuscript; available in PMC: 2018 Sep 1.
Published in final edited form as: Genet Epidemiol. 2017 Jun 19;41(6):481–497. doi: 10.1002/gepi.22051

Table 5.

Significant shortest paths at amin = 0.3 and α1 = 0.001. Paths that include genome-wide significant SNPs were excluded. Pmarg, marginal association p-value. Pmult, multiple regression p-value applied to each path. SNPs in each path are ordered so that the first SNP is adjacent to the phenotype and the last SNP is tested for association. SNPs tested in each path are emphasized in bold.

Significant path CHR SNP BP Pmarg Pmult
1 5 rs2963327 8987159 2.0e-04 8.1e-08
1 5 rs2963345 8962508 3.2e-03 7.1e-03
1 5 rs6870451 8991885 9.3e-02 1.4e-06
2 5 rs2963327 8987159 2.0e-04 7.8e-08
2 5 rs2963344 8962428 3.7e-03 1.1e-02
2 5 rs6870451 8991885 9.3e-02 2.0e-06
3 5 rs2963327 8987159 2.0e-04 7.7e-08
3 5 rs2963345 8962508 3.2e-03 8.0e-03
3 5 rs11955429 8994715 7.8e-02 1.6e-06
4 5 rs2963327 8987159 2.0e-04 7.0e-08
4 5 rs2963344 8962428 3.7e-03 1.3e-02
4 5 rs11955429 8994715 7.8e-02 2.3e-06
5 5 rs2963337 8988632 1.5e-04 4.0e-08
5 5 rs2963345 8962508 3.2e-03 7.0e-03
5 5 rs6870451 8991885 9.3e-02 8.6e-07
6 5 rs2963337 8988632 1.5e-04 3.9e-08
6 5 rs2963344 8962428 3.7e-03 1.1e-02
6 5 rs6870451 8991885 9.3e-02 1.3e-06
7 5 rs2963337 8988632 1.5e-04 3.8e-08
7 5 rs2963345 8962508 3.2e-03 7.9e-03
7 5 rs11955429 8994715 7.8e-02 9.9e-07
8 5 rs2963337 8988632 1.5e-04 3.5e-08
8 5 rs2963344 8962428 3.7e-03 1.2e-02
8 5 rs11955429 8994715 7.8e-02 1.4e-06