Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs687621
ABO
0.851 0.240 9 133261662 intron variant G/A;C snv 11
rs10739217
LOC107987108
0.925 0.040 9 105973112 regulatory region variant T/A;C snv 3
rs11190870 0.827 0.200 10 101219450 intergenic variant T/A;C snv 3
rs1828853
MIR4300HG
0.925 0.040 11 82371520 intron variant G/A;C;T snv 3
rs7741741
ADGRG6
0.925 0.040 6 142334664 intron variant T/A;G snv 3
rs10019193
LOC107986198 ; DDX60L ; PALLD
0.925 0.040 4 168526369 intron variant G/A;C snv 2
rs10059423
CTNND2
0.925 0.040 5 11600827 intron variant A/C;T snv 2
rs10175478
LINC01122
0.925 0.040 2 58913731 intron variant C/A;T snv 2
rs1024036
KIF9
0.925 0.040 3 47276175 intron variant T/A;C;G snv 2
rs10242233 0.925 0.040 7 118986159 intergenic variant T/C;G snv 2
rs10259477 0.925 0.040 7 11855801 intergenic variant A/C;T snv 2
rs10280201 0.925 0.040 7 38637079 intergenic variant G/A;T snv 2
rs1028911
LOC100506207 ; HULC
0.925 0.040 6 8706288 intron variant T/C;G snv 2
rs1046774
ZMAT1
0.925 0.040 X 101882824 3 prime UTR variant G/A;T snv 2
rs10753165 0.925 0.040 1 177602999 intron variant T/A;G snv 2
rs10757483 0.925 0.040 9 24732826 intergenic variant T/A;C snv 2
rs10809558 0.925 0.040 9 11701596 intron variant C/G;T snv 2
rs10843459
LOC105369649
0.925 0.040 12 9343806 upstream gene variant C/G;T snv 2
rs10910445
SIPA1L2
0.925 0.040 1 232421037 intron variant T/A;C snv 2
rs10919410
GORAB-AS1
0.925 0.040 1 170460651 non coding transcript exon variant T/A;G snv 2
rs10920828 0.925 0.040 1 190884663 intron variant G/A;C;T snv 2
rs11019290
OSBPL9P3
0.925 0.040 11 91115993 non coding transcript exon variant C/A;T snv 2
rs11019759 0.925 0.040 11 92050584 intergenic variant G/A;C snv 2
rs11020496
GRM5
0.925 0.040 11 88576138 intron variant C/A;T snv 2
rs11089671 0.925 0.040 22 34434612 intergenic variant A/C;G;T snv 2