Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10001106 0.925 0.120 4 10125817 intergenic variant T/A;C snv 3
rs1000113
IRGM
0.925 0.040 5 150860514 intron variant C/T snv 0.13 1
rs10001632
CLNK ; LOC105374482
0.925 0.120 4 10520247 intron variant A/C snv 0.97 2
rs10001964
SLC2A9
0.925 0.120 4 9957651 intron variant C/T snv 0.48 3
rs10002268 1.000 0.080 4 55653725 intergenic variant T/C snv 0.41 1
rs10002630
LOC107986195
4 148737523 intron variant G/C snv 0.31 1
rs10002984 0.925 0.120 4 9679109 intron variant T/C snv 0.95 2
rs10003001
SLC2A9
0.925 0.120 4 9982851 intron variant C/T snv 0.21 3
rs10003632
IQCM
4 149563756 missense variant G/T snv 4.1E-02 1
rs10003864 0.925 0.120 4 10435767 downstream gene variant T/C snv 0.29 3
rs10004195
TLR10
0.790 0.320 4 38783103 upstream gene variant T/A snv 0.29 1
rs10004908 4 87886094 intergenic variant G/A snv 0.70 1
rs10004961
LOC107986195
4 148743746 intron variant C/T snv 0.24 1
rs10005684 0.925 0.120 4 9625273 intron variant T/A;G snv 2
rs1000579
STX18-AS1
1.000 0.080 4 4717767 intron variant A/G snv 0.44 1
rs1000597 0.925 0.120 7 30897563 intron variant T/A;C snv 1
rs10006397
SLC2A9
0.925 0.120 4 10034516 non coding transcript exon variant C/A snv 0.78 3
rs1000662 0.925 0.120 11 64466347 intergenic variant G/A snv 0.60 2
rs1000668
TMC1
9 72790943 intron variant T/A;G snv 1
rs10007186
LINC01094
4 78667891 intron variant C/T snv 0.65 1
rs10007469 0.925 0.120 4 9731119 upstream gene variant G/A;C;T snv 2
rs10007754
TACR3
4 103706285 intron variant T/G snv 0.34 1
rs1000778
FADS3
1.000 0.040 11 61887833 intron variant A/G snv 0.59 2
rs10008035
SLC2A9 ; LOC105374476
0.925 0.120 4 9997711 intron variant G/A;T snv 3
rs10008491
LOC107986195
4 148731957 intron variant A/G snv 0.31 1