Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 10
rs886424
LINC00243
0.776 0.320 6 30814225 non coding transcript exon variant C/T snv 7.1E-02 8.7E-02 7
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 6
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 6
rs4650608 0.851 0.040 1 78772330 intergenic variant T/C snv 0.29 5
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 5
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 4
rs13211507
PGBD1
0.882 0.200 6 28289600 intron variant T/C snv 6.4E-02 4
rs17693963 0.882 0.040 6 27742386 upstream gene variant A/C;G snv 3
rs9834970 0.790 0.080 3 36814539 downstream gene variant T/C snv 0.45 3
rs10994359
ANK3
0.827 0.040 10 60462349 intron variant T/C snv 8.0E-02 3
rs2524005
HLA-A
0.882 0.160 6 29931900 upstream gene variant G/A snv 0.18 3
rs10275045
MAD1L1
0.882 0.160 7 1881190 intron variant C/T snv 0.35 3
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 3
rs4356203
PIK3C2A
0.925 0.040 11 17138601 intron variant A/G snv 0.31 3
rs2251219
SMIM4 ; PBRM1
0.732 0.120 3 52550771 synonymous variant T/C;G snv 0.39; 4.0E-06 0.34 3
rs1009080 1 29958713 intergenic variant G/A snv 0.54 2
rs10949808 7 156255955 intergenic variant T/G snv 0.45 2
rs12201676 0.925 0.040 6 89022382 regulatory region variant T/C snv 0.21 2
rs12527359 6 89018502 intergenic variant T/A snv 0.23 2
rs12807809 0.882 0.160 11 124736389 upstream gene variant T/C snv 0.20 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