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. 2011 Jan 30;122(7):1363–1373. doi: 10.1007/s00122-011-1537-4

Table 2.

Significant SNP markers, with QTL map positions

Trait SNP Chrom Position Interval (nra) −log10 (fp) % σg2 Effect s.e.
Yield 11_10191 2H 63.53 63.53 (3) 3.15 8.29 0.18 0.05
11_11348 7H 70.4 70.4 (1) 3.26 10.99 0.14 0.04
11_11445 7H 84.92 84.92 (1) 3.05 10.46 −0.12 0.04
Heading date 11_10357 1H 100.69 100.69 (1) 3.07 6.84 1.78 0.53
11_20438 2H 63.53 63.53 (9) 4.95 10.91 −3.70 0.84
11_20366 2H 128.26 128.26 (1) 3.11 6.88 2.11 0.59
11_11401 3H 58.01 58.01 (1) 3.42 7.07 1.84 0.55
11_11090 5H 132.63 132.63 (1) 3.32 6.60 2.59 0.74
Harvest index Height 11_20603 1H 135.56 135.56 (1) 3.27 11.00 −0.52 0.16
11_10191 2H 63.53 63.53 (3) 3.64 10.38 0.98 0.27
11_10918 3H 123.68 123.68 (1) 2.95 12.68 0.52 0.16
11_10376 2H 131.77 131.77 (1) 3.39 8.05 1.53 0.43
11_20894 5H 2.09 2.09 (1) 2.91 6.09 −1.68 0.52
Thousand kernel weight Grains per spike 11_10796 2H 58.24 58.24 (3) 4.21 9.86 −2.18 0.54
11_10213 2H 86.63 86.63 (1) 3.08 5.21 −1.50 0.45
11_20680 4H 26.19 24.59–26.19 (2) 3.49 6.85 2.25 0.62
11_20121 1H 75.45 75.45 (1) 2.94 8.88 1.36 0.42
11_10436 2H 62.82 62.82 (1) 3.16 9.01 2.06b 0.61
11_10287 2H 85.92 82.75–86.63 (3) 4.85 14.86 2.28 0.52
11_21453 2H 155.3 155.3 (2) 3.28 8.89 −1.36 0.39
11_20422 4H 24.59 24.59–26.19 (8) 14.35 41.35 4.15 0.53
11_20610 4H 54.25 54.25–54.98 (3) 3.42 10.42 1.95 0.55
11_20732 4H 92.38 92.38 (1) 4.08 14.69 −1.57 0.39
Spikes per m2 11_20422 4H 24.59 24.59–26.19 (5) 4.93 29.52 −20.8 4.74
11_20553 5H 2.81 2.81 (1) 3.14 12.38 10.54 3.12

Number of significant SNP markers and a genetic position range is provided when more than one significant SNP was present. −log10 (p value), percentage of explained genetic variance (σ2g), effect size and standard error of the effect are shown only for the most significant marker within the interval

aNumber of significant SNP markers within the positive interval

bSNPs not in phase with neighbour SNPs linked to QTL for other yield components traits. Direction of genetic effects is based on the base calling of the individual SNPs, which does not necessarily reflect the haplotypes linked to the causal variants