Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs643507
LPIN2 ; CHORDC1P4
1.000 0.080 18 2946293 non coding transcript exon variant C/T snv 0.96 0.92 1
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 6
rs215607
PDE1C
7 32298725 missense variant G/A snv 0.79 0.77 1
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 7
rs2904880
CD19 ; RABEP2
1.000 0.040 16 28933075 missense variant C/G snv 0.72 0.76 2
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs5219
KCNJ11
0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 2
rs5215
KCNJ11
0.827 0.160 11 17387083 missense variant C/T snv 0.64 0.71 2
rs11042023
TRIM66
1.000 0.080 11 8640969 missense variant T/C snv 0.60 0.59 1
rs2307111
POC5
0.925 0.120 5 75707853 missense variant T/A;C snv 4.5E-06; 0.47 1
rs11676272
ADCY3
1.000 0.040 2 24918669 missense variant A/G snv 0.47 0.57 2
rs1064213
PLCL1
2 198085516 missense variant G/A snv 0.44 0.41 1
rs591120
CRYZL2P-SEC16B ; SEC16B
1 177933618 missense variant G/A;C snv 4.0E-06; 0.42 2
rs4985155
PDXDC1
16 15035602 intron variant A/G snv 0.40 0.37 2
rs8049439
ATXN2L
0.925 0.120 16 28826194 intron variant T/C;G snv 0.38 2
rs7200543
PDXDC1
16 15036113 synonymous variant A/G snv 0.35 0.30 4
rs7498665
SH2B1
0.925 0.120 16 28871920 missense variant A/G;T snv 0.35 5
rs6235
LOC101929710 ; PCSK1
0.925 0.120 5 96393194 missense variant C/G snv 0.26 0.23 1
rs1426654
SLC24A5 ; MYEF2
1.000 15 48134287 missense variant A/G;T snv 0.23 1
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 4
rs11672660
GIPR ; MIR642B
19 45676926 intron variant C/T snv 0.18 0.17 2
rs1800437
GIPR
0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 1
rs2287019
QPCTL
1.000 0.080 19 45698914 intron variant C/T snv 0.17 0.16 2
rs4432245
EIF2AK4
15 40032280 intron variant T/C snv 0.15 0.12 2
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20