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. 2018 Oct 11;8:15164. doi: 10.1038/s41598-018-33327-9

Table 2.

Suggestive SNPs detected for methane production with Bayesian Factor 10 < BF < 30, their position in base pairs, minor allele frequency (MAF) and percentage of total genetic variance explained by them.

BTA SNP name Position (bp) MAF BF Allele sub. effecta Total genetic var. expl. (%)
1 ARSBFGLNGS94761 53656600 0.416 11.22 0.088 0.003
1 ARSBFGLNGS3821 61286751 0.337 15.37 0.177
1 BTB01665387 63061634 0.437 12.26 0.231
1 ARSBFGLNGS4572 67212088 0.381 28.01 0.179
2 Hapmap44041BTA23382 10617894 0.266 15.37 0.200 0.001
3 Hapmap33584BTA141202 30922247 0.128 10.19 0.235 0.075
3 Hapmap44183BTA105889 37602383 0.428 14.33 0.172
3 ARSBFGLNGS38388 43476846 0.421 11.22 0.170
3 ARSBFGLNGS98870 98587436 0.428 16.41 0.114
3 Hapmap39765BTA62582 99317016 0.266 13.29 0.225
4 BTA72259nors 20510260 0.360 17.45 0.172 0.001
8 Hapmap26798BTA82382 11398105 0.191 11.22 0.207 0.012
8 BTB00863195 23634451 0.449 10.19 0.088
8 ARSBFGLNGS39902 24288969 0.404 17.45 0.114
8 Hapmap52006BTA77999 29628947 0.449 15.37 0.133
8 BTB01356348 34847992 0.280 11.22 0.185
9 UAIFASA4057 50279445 0.245 16.41 0.197 0.005
9 BTB00392496 50899854 0.322 21.65 0.155
9 BTB01520203 62539556 0.383 22.70 0.166
9 Hapmap58377rs29014990 66292441 0.353 18.50 0.179
9 Hapmap42705BTA85041 99135245 0.196 16.41 0.191
10 BTA59410nors 17730891 0.215 12.26 0.194 0.002
11 ARSBFGLNGS27959 22465305 0.128 12.26 0.161 0.004
11 BTB01397452 33167082 0.428 21.65 0.156
11 BTB01641011 33771048 0.486 10.19 0.117
12 BTA31817nors 22219373 0.241 11.22 0.289 0.001
15 ARSBFGLNGS86665 67556240 0.227 16.41 0.196 0.003
18 ARSBFGLNGS14182 33602408 0.323 12.26 0.144 0.001
19 Hapmap48676BTA18047 47374363 0.490 13.29 0.094 0.003
20 ARSBFGLBAC36856 63407185 0.356 23.76 0.129 0.001
23 Hapmap61132rs29019650 11907305 0.402 10.19 0.158 0.001
24 ARSBFGLBAC31288 4273189 0.178 20.60 0.242 0.002
25 ARSBFGLNGS114786 7952738 0.400 10.19 0.141 0.002
28 BTB00987935 35294673 0.400 21.65 0.169 0.005

aAllele substitution effects were estimated as α=σa2(2pq)1, where σa2 is the genetic variance explained by the SNP, and p and q are the frequencies of the two alleles76.