Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10692845 2 21070463 regulatory region variant -/GA;GACTCAAAGTACACATTTCCTAGA delins 0.69 1
rs147010738 13 72193030 intergenic variant -/GT;GTGT ins 1
rs3832016
CELSR2
1 109275536 3 prime UTR variant -/T ins 0.74 1
rs68055275
ST3GAL4
11 126369248 intron variant -/T;TT delins 3
rs145976573
LOC105378286 ; MARCHF8
10 45483784 intron variant -/TGTTAAGTCAAATAA;TGTTAAGTGAAATAA delins 1
rs145955280
EVI5
1 92671973 intron variant A/-;AA;AAA delins 2
rs2980853 0.851 0.120 8 125466108 upstream gene variant A/C snv 0.43 16
rs2740488
ABCA1
0.827 0.120 9 104899461 intron variant A/C snv 0.29 9
rs17030613
CAPZA1
1 112648185 intron variant A/C snv 0.19 6
rs4665710 2 20998163 downstream gene variant A/C snv 0.76 5
rs1797912
PPARG
1.000 0.040 3 12428740 intron variant A/C snv 0.33 2
rs496800 1 234715469 intron variant A/C snv 0.65 2
rs557933 1 234717521 intron variant A/C snv 0.65 2
rs74551598
WHRN
9 114415286 intron variant A/C snv 0.20 2
rs1469149
CSF2
5 132073149 upstream gene variant A/C snv 0.39 1
rs2737229
TRPS1
8 115636338 intron variant A/C snv 0.48 1
rs585967 1.000 0.040 2 21047682 upstream gene variant A/C snv 0.81 1
rs7203984
CETP
16 56965346 intron variant A/C snv 0.31 1
rs7849420
MIR31HG
9 21499625 intron variant A/C snv 0.65 1
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 7
rs1801689
APOH
17 66214462 missense variant A/C;G snv 4.0E-06; 2.4E-02; 4.8E-05 5
rs77960347
LIPG
18 49583585 missense variant A/C;G snv 4.0E-06; 8.7E-03 5
rs11207995
DOCK7
1 62583880 intron variant A/C;G snv 3
rs5471
TXNL4B ; HP
0.882 0.160 16 72054562 5 prime UTR variant A/C;G snv 7.9E-03 3
rs10412048 19 11083273 downstream gene variant A/C;G snv 2