Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs117542855 1.000 0.040 11 1635713 regulatory region variant C/G;T snv 3.1E-02 1
rs1953124 1.000 0.040 13 65771915 regulatory region variant C/A;G;T snv 1
rs222054 1.000 0.040 4 71738582 downstream gene variant C/G snv 0.27 1
rs497408 1.000 0.040 6 23993395 regulatory region variant C/A;T snv 1
rs5748926 1.000 0.040 22 17168884 upstream gene variant T/C snv 0.70 1
rs6499186 1.000 0.040 16 68626662 downstream gene variant C/T snv 0.84 1
rs698718 1.000 0.040 16 68526282 upstream gene variant A/C;G;T snv 1
rs71413689 1.000 0.040 2 150398953 intergenic variant G/A snv 1.7E-02 1
rs72943235 1.000 0.040 2 88201127 intergenic variant G/A snv 9.0E-02 1
rs4149267
ABCA1
1.000 0.040 9 104889664 intron variant T/C snv 0.47 1
rs6128907
ACTR5
1.000 0.040 20 38759219 intron variant T/C snv 0.17 1
rs1492100
AGTR1
1.000 0.040 3 148719640 intron variant T/A snv 0.34 1
rs2276736
AGTR1
1.000 0.040 3 148708086 intron variant A/G;T snv 1
rs3772627
AGTR1
1.000 0.040 3 148712467 intron variant A/G snv 0.44 1
rs3772630
AGTR1
1.000 0.040 3 148708685 intron variant T/C snv 0.44 1
rs3772633
AGTR1
1.000 0.040 3 148700381 intron variant T/C snv 0.13 1
rs17120035
APOA5
1.000 0.040 11 116793135 upstream gene variant C/T snv 6.4E-02 1
rs768007422
ARHGEF7
1.000 0.040 13 111277667 missense variant C/G snv 1
rs762049291
CCR2
1.000 0.040 3 46358410 missense variant A/G;T snv 4.0E-06; 4.0E-06 1
rs537635771
CD40
1.000 0.040 20 46128178 missense variant C/G;T snv 1
rs2303861
CD82
1.000 0.040 11 44618466 intron variant A/G snv 0.73 1
rs6843722
CLOCK
1.000 0.040 4 55465165 intron variant A/C snv 0.30 1
rs1805074
DMGDH
1.000 0.040 5 79028529 missense variant A/G snv 0.27 0.33 1
rs12373751
ERBB4
1.000 0.040 2 212072166 intron variant T/C snv 0.62 1
rs1858999
GATAD2A
1.000 0.040 19 19386860 intron variant C/G snv 0.56 1