Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 4
rs301807 0.925 0.080 1 8424763 intron variant A/G;T snv 4
rs301819 0.882 0.120 1 8441726 intron variant A/G;T snv 3
rs78037977 0.925 0.120 1 172746562 upstream gene variant A/G snv 7.9E-02 2
rs16843742 1.000 0.040 1 198703170 intron variant T/C;G snv 1
rs4908760 1.000 0.040 1 8466082 intron variant G/A snv 0.68 1
rs2111485 0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46 12
rs10200159 1.000 0.040 2 55617974 non coding transcript exon variant T/C snv 0.14 1
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 1
rs199559999 1.000 0.040 2 191090480 intron variant TAC/- del 1
rs231725 0.851 0.240 2 203875952 downstream gene variant G/A snv 0.38 1
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 1
rs41342147 1.000 0.040 2 241468173 missense variant G/A;T snv 0.11; 8.0E-06 1
rs4308124 1.000 0.040 2 111252909 intron variant T/C snv 0.44 1
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv 2
rs13076312
LPP
1.000 0.040 3 188371466 intron variant C/T snv 0.44 1
rs148136154 1.000 0.040 3 119564621 intergenic variant T/C;G snv 1
rs34346645 1.000 0.040 3 71508794 intron variant C/A snv 0.32 1
rs35161626 1.000 0.040 3 23470822 intron variant A/- del 0.64 1
rs59374417 0.925 0.040 3 119569567 intergenic variant A/C;T snv 1
rs6583331 1.000 0.040 3 196620382 intergenic variant T/A snv 0.38 1
rs9851967
LPP
1.000 0.040 3 188369840 intron variant C/T snv 0.35 1
rs16872571 0.925 0.080 4 10725229 intergenic variant C/T snv 0.33 2
rs1031034 1.000 0.040 4 101302229 intron variant C/A snv 0.29 1