Disease: High density lipoprotein measurement
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11216126 1.000 0.040 11 116746524 downstream gene variant A/C snv 0.11 3
rs2740488
ABCA1
0.827 0.120 9 104899461 intron variant A/C snv 0.29 9
rs2980853 0.851 0.120 8 125466108 upstream gene variant A/C snv 0.43 16
rs4665710 2 20998163 downstream gene variant A/C snv 0.76 5
rs7519429
DNM3 ; PIGC
1 172380106 intron variant A/C snv 0.29 2
rs11765979
LOC105375508
7 130761118 intergenic variant A/C;G snv 2
rs150844304
TP53BP1
15 43434427 intron variant A/C;G snv 4
rs2322549
INPP4B
4 142395874 intron variant A/C;G snv 2
rs2943646 2 226234818 intergenic variant A/C;G snv 3
rs2980875 8 125469505 intron variant A/C;G;T snv 4
rs9863753
STAB1
3 52495883 intron variant A/C;G;T snv 2
rs180349 0.925 0.200 11 116741111 intergenic variant A/C;T snv 3
rs10185855
TBC1D8
2 101025798 intron variant A/G snv 0.35 4
rs1077835
ALDH1A2 ; LIPC
15 58431227 intron variant A/G snv 0.34 3
rs10864728
GALNT2
1 230169168 intron variant A/G snv 0.50 3
rs1129555
GPAM
10 112150963 3 prime UTR variant A/G snv 0.71 5
rs12579302
ATP2B1
0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs12678919 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 3
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 18
rs174554
FADS1 ; FADS2
1.000 0.080 11 61811991 intron variant A/G snv 0.40 0.28 6
rs174566
FADS1 ; FADS2
0.925 0.160 11 61824890 intron variant A/G snv 0.34 7
rs193084249 1 26661155 intergenic variant A/G snv 1.7E-02 3
rs2035403
AFF1
4 87097839 intron variant A/G snv 0.35 2
rs2083637 0.925 0.080 8 20007664 intergenic variant A/G snv 0.25 3
rs2169387
LOC157273
8 9323885 intron variant A/G snv 0.87 6