Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs667920
STAG1
1.000 0.040 3 136350630 intron variant G/T snv 0.78 1
rs606452
SERPINH1
1.000 0.040 11 75565133 intron variant A/C snv 0.78 3
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 4
rs1250229 1.000 0.040 2 215439661 upstream gene variant T/C snv 0.77 3
rs7809950
BCAP29
1.000 0.040 7 107597362 intron variant T/C snv 0.77 1
rs6001960
MRTFA
1.000 0.040 22 40547028 intron variant A/G snv 0.77 1
rs895953
SETD1B
1.000 0.040 12 121811142 intron variant G/T snv 0.76 5
rs6544713
ABCG8
0.925 0.040 2 43846742 non coding transcript exon variant T/C snv 0.75 3
rs3775058
UNC5C
1.000 0.040 4 95196220 intron variant A/T snv 0.75 1
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 10
rs1623003
NPC1
1.000 0.040 18 23585199 intron variant C/T snv 0.74 1
rs944172
LOC105376208
1.000 0.040 9 107755513 TF binding site variant C/T snv 0.73 1
rs515135 0.807 0.160 2 21063185 intergenic variant T/C snv 0.73 3
rs644045
CYP21A2 ; C2
0.851 0.240 6 31916180 intron variant A/G snv 0.72 2
rs2972146 0.882 0.040 2 226235982 intergenic variant G/T snv 0.72 6
rs2189839
BCAP29
1.000 0.040 7 107589581 intron variant A/G snv 0.72 1
rs3931020 0.882 0.040 1 74769633 downstream gene variant T/C snv 0.71 1
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 1
rs668948 1.000 0.040 2 21068657 regulatory region variant G/A snv 0.71 4
rs7617773 1.000 0.040 3 48152025 TF binding site variant C/T snv 0.71 1
rs2650000
HNF1A-AS1
0.851 0.200 12 120951159 intron variant A/C snv 0.70 2
rs4646248 1.000 0.040 8 18402845 downstream gene variant C/T snv 0.70 1
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 10
rs1801253
ADRB1
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 6
rs1550115
ADCY3 ; CENPO
1.000 0.040 2 24818751 intron variant C/T snv 0.69 1