Disease: Serum HDL cholesterol measurement
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10019888 4 26061368 regulatory region variant A/G snv 0.17 2
rs10096633 1.000 0.040 8 19973410 regulatory region variant C/T snv 0.22 7
rs103294 0.827 0.200 19 54293995 downstream gene variant T/C snv 0.82 3
rs10503669 0.925 0.080 8 19990179 intergenic variant C/A snv 8.4E-02 7
rs10808546 8 125483576 intron variant C/T snv 0.39 4
rs1084651 6 160668785 intron variant G/A snv 0.23 2
rs11216126 1.000 0.040 11 116746524 downstream gene variant A/C snv 0.11 2
rs11246602 11 54607190 upstream gene variant A/G snv 0.11 2
rs11819350 10 17133943 upstream gene variant C/G;T snv 2
rs11902417 2 20976028 intergenic variant G/A snv 0.25 7
rs11986942 1.000 0.040 8 20009934 intergenic variant C/G;T snv 4
rs12097137 1 101243889 downstream gene variant G/A;T snv 3
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 10
rs12678919 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 7
rs12708967 16 56959299 upstream gene variant T/C snv 0.18 4
rs12720917 16 56985480 upstream gene variant T/C snv 0.10 2
rs12748152 1.000 0.120 1 26811902 upstream gene variant C/T snv 5.7E-02 5
rs12967135 18 60181790 intergenic variant G/A snv 0.24 3
rs1436424 16 56861122 upstream gene variant G/T snv 0.41 2
rs16860926 3 186609982 intron variant T/C snv 2.6E-02 4
rs16969352 15 39577083 upstream gene variant T/C snv 5.1E-02 2
rs17158782 5 100726979 intergenic variant T/C snv 1.9E-02 2
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 7
rs173539 0.882 0.080 16 56954132 intergenic variant C/T snv 0.33 7
rs17410914 8 19985951 intergenic variant C/A;T snv 4