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. 2013 Oct 1;3(10):1819–1825. doi: 10.1534/g3.113.007567

Table 2. Significant and suggestive QTL identified by genome-wide scan of F2 mice.

Trait QTLa Chr Peak cM 95% CI LODb Nearest marker Sex High Strain; Inheritance
HDL cholesterol Cq1c 1 74.7 70.6−81.6 8.9 rs13476229 MF KK, Add
2 36.2 21.2−51.2 3.1 rs3718711 M I, Add
3 19.2 17.2−38.2 3.4 rs6324747 F I, Add
4 75.1 60.1−88.6 3.1 UT_4_132.137715 F KK, Add
6 24.8 9.8−44.8 2.9 rs6355719 MF KK, Dom
Hdlq84 X 38.4 33.4−40.4 9.3 rs13483831 MF, M KK, Add
Non-HDL cholesterol Nhdlq13 1 67.7 56.7−78.7 3.2 rs6185344 MF, F KK, Rec
Nhdlq14 3 32.4 29.2−35.2 4.5 rs6198234 MF Het, UDom
5 42.8 23.8−55.8 2.3 rs3667334 F KK, Dom
7 64.0 50.0−79.0 2.3 rs13479455 F I, Add
14 41.9 19.9−54.9 2.2 rs6156908 F KK, Add
X 38.3 18.4−61.4 3.3 rs13483831 MF, F KK, Add

QTL, quantitative trait loci; CI, confidence interval; LOD, logarithm of the odds ratio; HDL, high-density lipoprotein.

a

QTL were named if they were significant or if they were suggestive but confirmed QTL reported previously.

b

Significant LOD scores were determined by 1000 permutations for the autosomes and 16,803 permutations for Chr X and are indicated in bold.

c

Apoa2 is the likely causative gene.