Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12061601 1.000 0.040 1 169101212 intron variant T/C snv 0.16 3
rs2070016
FGA
1.000 0.040 4 154589162 intron variant A/G snv 0.12 3
rs253
LPL
1.000 0.040 8 19953906 intron variant C/T snv 0.53 3
rs17645023 1.000 0.040 17 66920916 intergenic variant A/T snv 0.22 2
rs1975802
PLA2G15
1.000 0.040 16 68251944 intron variant A/C;G snv 2
rs2312147
VRK2
1.000 0.040 2 57995793 intron variant T/C snv 0.70 2
rs4654748
NBPF3
1.000 0.040 1 21459575 intron variant C/T snv 0.38 2
rs4657175
NOS1AP
1.000 0.040 1 162225948 intron variant T/C;G snv 2
rs4949526 1.000 0.040 1 29959372 intergenic variant T/C snv 0.54 2
rs6589386 1.000 0.040 11 113573031 intergenic variant C/T snv 0.36 2
rs6913660 1.000 0.040 6 27123646 upstream gene variant C/A snv 0.14 2
rs6932590 1.000 0.040 6 27281152 downstream gene variant T/C snv 0.26 2
rs7359397
SH2B1
1.000 0.040 16 28874338 upstream gene variant C/T snv 0.28 2
rs7863476
PLAA
1.000 0.040 9 26915927 intron variant G/A;C snv 0.29 2
rs1001684 1.000 0.040 5 40810324 intergenic variant C/A snv 0.29 1
rs1002424
PRKAA1
1.000 0.040 5 40767295 intron variant A/G snv 0.31 1
rs10065570
RPL37
1.000 0.040 5 40835525 upstream gene variant C/T snv 0.33 1
rs10135277 1.000 0.040 14 35354025 TF binding site variant C/T snv 0.43 1
rs10140896
EML5
1.000 0.040 14 88752194 intron variant C/A;G;T snv 1
rs10155413
LINC02511
1.000 0.040 4 137116128 intron variant T/C snv 0.35 1
rs10226475
MAD1L1
1.000 0.040 7 2186527 intron variant A/G snv 0.34 1
rs1025641
C10orf90
1.000 0.040 10 126618623 intron variant T/C snv 0.43 1
rs1035130
IL18R1
1.000 0.040 2 102384942 synonymous variant C/T snv 0.26 0.24 1
rs10429924 1.000 0.040 1 244227262 intergenic variant C/T snv 8.8E-02 1
rs10498146 1.000 0.040 2 222987318 intergenic variant A/G snv 6.2E-02 1