Disease: Serum total cholesterol measurement
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10054063 5 173965395 downstream gene variant A/T snv 0.26 4
rs10808546 8 125483576 intron variant C/T snv 0.39 6
rs112875651 8 125494452 intron variant G/A snv 0.31 7
rs12130333 1.000 0.080 1 62726106 regulatory region variant C/T snv 0.16 2
rs12272004 1.000 0.040 11 116733008 TF binding site variant C/A snv 9.8E-02 4
rs12310617 0.851 0.120 12 3060327 intergenic variant C/T snv 0.11 16
rs12420422 0.851 0.120 11 123009573 intergenic variant G/A snv 3.4E-02 16
rs1260333 0.882 0.160 2 27525757 downstream gene variant A/G snv 0.58 2
rs13392272 2 20994618 downstream gene variant C/T snv 0.37 4
rs1495741 0.827 0.240 8 18415371 regulatory region variant G/A snv 0.71 5
rs1495743 8 18415790 intergenic variant G/A;C snv 4
rs1501908 1.000 0.040 5 156971158 intergenic variant G/A;C;T snv 3
rs1558861 11 116736721 regulatory region variant C/G;T snv 4
rs17140821 0.851 0.120 7 19177581 regulatory region variant G/A snv 7.9E-02 16
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 18
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 3
rs173539 0.882 0.080 16 56954132 intergenic variant C/T snv 0.33 6
rs176813 4 68733813 regulatory region variant T/C snv 0.38 4
rs180349 0.925 0.200 11 116741111 intergenic variant A/C;T snv 3
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 7
rs2068888 10 93079885 downstream gene variant G/A snv 0.42 5
rs2207132 20 40513876 intergenic variant G/A snv 2.7E-02 4
rs222826 0.851 0.120 2 146120964 regulatory region variant T/C snv 0.94 16
rs2367970 11 116710925 intergenic variant G/A snv 0.22 3
rs2452170 19 48710247 downstream gene variant G/A;C snv 3