Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17145750
MLXIPL
0.925 0.120 7 73612048 intron variant C/A;T snv 7
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 6
rs115810
TRIM38
0.925 0.120 6 25975655 intron variant G/A;C snv 5
rs1540276
H4C2
0.925 0.120 6 26028591 upstream gene variant T/A;G snv 5
rs199734 0.925 0.120 6 25940165 intergenic variant G/A;C snv 5
rs199737 0.925 0.120 6 25933310 upstream gene variant A/C;T snv 5
rs386406569 0.925 0.120 6 26101212 upstream gene variant -/C delins 5
rs807212 0.925 0.120 6 26065393 regulatory region variant A/G;T snv 5
rs10946785
CARMIL1
0.925 0.120 6 25616840 intron variant G/A;T snv 4
rs1165151
SLC17A1
0.925 0.120 6 25821388 intron variant T/A;G snv 4
rs1165152
SLC17A1
0.925 0.120 6 25818538 intron variant A/C;G;T snv 4
rs1165153
SLC17A1
0.925 0.120 6 25817561 intron variant A/G;T snv 4
rs1165205
SLC17A3
0.925 0.120 6 25870314 intron variant T/A;G snv 4
rs1184804
SLC17A3
0.925 0.120 6 25867998 intron variant T/A;C snv 4
rs1185567
SLC17A1
0.925 0.120 6 25818360 intron variant A/G;T snv 4
rs150551
CARMIL1
0.925 0.120 6 25533702 intron variant A/G;T snv 4
rs1540275 0.925 0.120 6 26036248 upstream gene variant T/A;C snv 4
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 4
rs4072037
MUC1
0.732 0.240 1 155192276 splice acceptor variant C/A;T snv 0.59 4
rs6903765
CARMIL1
0.925 0.120 6 25609510 intron variant A/G;T snv 4
rs6905614
SLC17A3
0.925 0.120 6 25840257 intron variant C/A;G snv 4
rs734553
SLC2A9
0.851 0.240 4 9921380 intron variant G/A;T snv 4
rs737267
SLC2A9
0.851 0.240 4 9933120 intron variant G/A;T snv 4
rs765285
SLC17A1
0.925 0.120 6 25828014 intron variant G/C;T snv 4
rs7761700
CARMIL1
0.925 0.120 6 25617963 intron variant G/C;T snv 4