Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4932373
FES
1.000 0.040 15 90886057 intron variant A/C snv 0.25 2
rs2071382
FES
1.000 0.040 15 90884967 intron variant T/C snv 0.57 2
rs17514846
FURIN
0.882 0.120 15 90873320 intron variant C/A;G snv 5
rs57481061
ATP2B1
1.000 0.040 12 89625401 intron variant C/G snv 0.14 1
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv 7
rs2681472
ATP2B1
0.882 0.080 12 89615182 intron variant A/G snv 0.14 6
rs1051338
LIPA
0.807 0.120 10 89247603 missense variant T/G snv 0.32 0.26 1
rs2246942
LIPA
0.925 0.040 10 89245129 intron variant A/C;G snv 1
rs1412444
LIPA
0.851 0.120 10 89243170 intron variant C/T snv 0.37 2
rs2083460 1.000 0.040 15 89031253 intergenic variant T/C;G snv 1
rs8042271 0.882 0.040 15 89030987 intergenic variant G/A;T snv 1
rs1807214 1.000 0.040 15 89022026 regulatory region variant A/C snv 0.29 1
rs139401390 0.851 0.120 10 88643382 regulatory region variant A/G snv 1.0E-02 3
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 5
rs61403071 1.000 0.040 16 86666118 intron variant C/G;T snv 1
rs1561198
VAMP5
0.882 0.120 2 85582866 upstream gene variant C/T snv 0.52 1
rs7568458
GGCX
1.000 0.040 2 85561052 intron variant T/A;C snv 1
rs2028900
MAT2A ; PARTICL
1.000 0.040 2 85540612 intron variant C/T snv 0.50 1
rs6743030 1.000 0.040 2 85536397 upstream gene variant C/T snv 0.51 1
rs2166529 1.000 0.040 2 85515052 intergenic variant G/A;T snv 1
rs2880765
AKAP13
1.000 0.040 15 85513231 intron variant A/T snv 0.48 1
rs59372292
HNRNPM
1.000 0.040 19 8481254 intron variant C/T snv 0.16 1
rs9362054
LOC107986620 ; LINC01611
0.882 0.160 6 84468550 intron variant T/C snv 0.52 2
rs2967605
RAB11B
0.925 0.040 19 8404854 downstream gene variant C/T snv 0.20 1
rs116843064
ANGPTL4
0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02 7