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Table 2 Map and minor allele frequency information of each SNP randomly selected in the sprious pleiotropy simulation presented in Listing 1, as well as those selected to be additive quantitative trait nucleotides (QTNs)

From: simplePHENOTYPES: SIMulation of pleiotropic, linked and epistatic phenotypes

Replication

Marker type

Marker

Allele

Chromosome

Position

\(\hbox {cM}^*\)

\(\hbox {MAF}^{**}\)

1

cause_of_LD

ss196453961

A/G

4

68,182,921

NA

0.50

1

cause_of_LD

ss196498075

A/G

10

87,305,008

NA

0.50

1

cause_of_LD

ss196495963

G/A

10

52,568,307

NA

0.50

1

QTN_upstream

ss196453979

G/A

4

68,369,212

NA

0.50

1

QTN_upstream

ss196498083

A/C

10

87,799,475

NA

0.50

1

QTN_upstream

ss196496034

G/A

10

54,432,827

NA

0.50

1

QTN_downstream

ss196453929

C/A

4

67,678,951

NA

0.50

1

QTN_downstream

ss196498065

A/G

10

87,189,608

NA

0.50

1

QTN_downstream

ss196496813

C/A

10

49,693,682

NA

0.50

  1. A value of \(''1''\) under the column labeled “Replication” indicates that these were the markers selected for the first experiment (i.e., the first replicate trait) for this genetic architecture
  2. \(^*\) centimorgan (This example does not contain information on genetic linkage).
  3. \(^{**}\) Marker data filtered by minor allele frequency (MAF) \(> 0.40\)