Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs145905715
RIC3 ; TUB
11 8100687 intron variant -/AT delins 3.5E-04 1
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 4
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 7
rs7203984
CETP
16 56965346 intron variant A/C snv 0.31 7
rs4665710 2 20998163 downstream gene variant A/C snv 0.76 6
rs16991720
KCNE1
21 34484464 intron variant A/C snv 4
rs585967 1.000 0.040 2 21047682 upstream gene variant A/C snv 0.81 4
rs3858076
ABCA1
9 104893841 intron variant A/C snv 0.20 3
rs1797912
PPARG
1.000 0.040 3 12428740 intron variant A/C snv 0.33 2
rs34515106
PLEK
2 68380846 missense variant A/C snv 6.7E-03 1.9E-03 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
rs7849420
MIR31HG
9 21499625 intron variant A/C snv 0.65 2
rs11597086
CHUK
10 100193948 non coding transcript exon variant A/C snv 0.30 0.29 1
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
rs556766
PIGO
9 35089051 3 prime UTR variant A/C snv 1.00 0.98 1