Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2431098 0.827 0.240 5 160460329 intron variant A/G;T snv 5
rs35929052 0.827 0.160 16 85960878 downstream gene variant C/G;T snv 5
rs112846137 0.851 0.160 3 160595133 intergenic variant G/T snv 5.3E-02 4
rs193107685 0.851 0.160 7 74123572 downstream gene variant T/C snv 1.0E-02 4
rs2736337 0.827 0.240 8 11484371 upstream gene variant T/C snv 0.26 4
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 4
rs3129843 0.827 0.160 6 32427949 intergenic variant A/G snv 6.3E-02 4
rs58721818 0.851 0.160 6 137922602 regulatory region variant C/G;T snv 4
rs744600 0.851 0.160 2 190700031 intron variant G/T snv 0.60 4
rs7929541 0.851 0.160 11 633689 upstream gene variant T/C snv 0.34 4
rs114042950 1.000 0.080 6 32699098 intergenic variant A/G snv 1
rs114388793 1.000 0.080 6 32699566 intergenic variant A/T snv 1
rs1815739
ACTN3
0.763 0.240 11 66560624 stop gained C/T snv 0.37 1
rs1217393
AP4B1-AS1
0.851 0.160 1 113891324 intron variant G/A snv 0.42 4
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs802791
ATG5
0.851 0.160 6 106121395 intron variant T/C snv 0.75 4
rs5754467
CCDC116 ; YDJC
0.851 0.160 22 21630805 upstream gene variant A/G;T snv 4
rs114050967
DDX39B ; ATP6V1G2-DDX39B ; SNORD117
1.000 0.080 6 31537703 intron variant A/G snv 1
rs9267488
DDX39B ; NFKBIL1 ; ATP6V1G2-DDX39B ; ATP6V1G2
1.000 0.080 6 31546470 splice region variant A/G snv 8.1E-02 9.9E-02 1
rs13101828
DGKQ
0.851 0.160 4 971932 intron variant A/G snv 0.43 6
rs6599390
DGKQ
1.000 0.080 4 962259 intron variant A/G snv 0.69 1
rs35677470
DNASE1L3
0.807 0.160 3 58197909 missense variant G/A;C snv 4.8E-02; 4.0E-06 5
rs114012716
HCP5
1.000 0.080 6 31466589 non coding transcript exon variant G/A snv 1
rs115146037
HCP5
1.000 0.080 6 31466554 non coding transcript exon variant A/T snv 1
rs115902351
HCP5
1.000 0.080 6 31466844 non coding transcript exon variant A/G snv 1