Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 25
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 21
rs4650608 0.851 0.040 1 78772330 intergenic variant T/C snv 0.29 5
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 5
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 5
rs2535629
ITIH3
0.827 0.040 3 52799203 intron variant G/A;C snv 5
rs6484218
CAND1.11 ; AMPD3
0.882 0.040 11 10369034 intron variant G/A snv 0.21 4
rs886424
LINC00243
0.776 0.320 6 30814225 non coding transcript exon variant C/T snv 7.1E-02 8.7E-02 4
rs17693963 0.882 0.040 6 27742386 upstream gene variant A/C;G snv 3
rs4949526 1.000 0.040 1 29959372 intergenic variant T/C snv 0.54 3
rs9834970 0.790 0.080 3 36814539 downstream gene variant T/C snv 0.45 3
rs10949808 7 156255955 intergenic variant T/G snv 0.45 2
rs11142387 9 70383416 downstream gene variant A/C snv 0.49 2
rs12201676 0.925 0.040 6 89022382 regulatory region variant T/C snv 0.21 2
rs17069122 6 108002555 downstream gene variant G/A snv 1.9E-02 2
rs17075286 3 43189231 intergenic variant C/G snv 5.9E-02 2
rs17645023 1.000 0.040 17 66920916 intergenic variant A/T snv 0.22 2
rs17746001 0.925 0.040 4 179734472 intergenic variant C/T snv 5.3E-02 2
rs1806864 9 87416754 regulatory region variant G/C snv 7.4E-02 2
rs2018368 11 10718819 intergenic variant C/G snv 0.59 2
rs2509843 11 98254676 intergenic variant A/C;G;T snv 2
rs2841307 6 100308811 intergenic variant C/T snv 0.20 2
rs4996815 13 105999312 intron variant G/T snv 0.61 2
rs6627057 X 145059799 downstream gene variant T/G snv 0.16 2
rs7727102 5 4720472 intron variant G/C snv 0.32 2