Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4377469
CCK
3 42261582 intron variant G/A;T snv 2
rs4715210 6 50929538 regulatory region variant C/G;T snv 2
rs4771122
MTIF3
1.000 0.080 13 27446043 intron variant G/A;C snv 2
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 2
rs4836133
LOC105379158 ; LINC02240
0.925 0.160 5 124996410 intron variant C/A;G;T snv 2
rs5219
KCNJ11
0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 2
rs591120
CRYZL2P-SEC16B ; SEC16B
1 177933618 missense variant G/A;C snv 4.0E-06; 0.42 2
rs7020996 0.925 0.120 9 22129580 downstream gene variant C/A;T snv 2
rs7923837 0.882 0.160 10 92722160 intergenic variant G/A;T snv 2
rs8049439
ATXN2L
0.925 0.120 16 28826194 intron variant T/C;G snv 0.38 2
rs8192472
CCK
3 42258378 intron variant C/G;T snv 2
rs9930333
FTO
0.882 0.120 16 53766065 intron variant T/C;G snv 2
rs10497870
NBEAL1
2 203105560 intron variant A/C;G snv 1
rs11658063
HNF1B
0.851 0.120 17 37743881 intron variant G/C;T snv 1
rs12454712
BCL2
0.925 0.120 18 63178651 intron variant T/A;C snv 1
rs1426654
SLC24A5 ; MYEF2
1.000 15 48134287 missense variant A/G;T snv 0.23 1
rs1582931 5 123321505 intergenic variant G/A;T snv 1
rs2145272 20 6645571 intergenic variant G/A;T snv 1
rs215634
PDE1C
7 32329536 intron variant A/G;T snv 1
rs2307111
POC5
0.925 0.120 5 75707853 missense variant T/A;C snv 4.5E-06; 0.47 1
rs2891403
RPH3A
1.000 0.040 12 112699767 intron variant A/G;T snv 1
rs3865188 0.790 0.320 16 82617112 intergenic variant A/G;T snv 1
rs4833407
ALPK1
1.000 0.080 4 112390634 intron variant C/A;T snv 1
rs6711012 1.000 0.080 2 624034 intergenic variant G/A;C;T snv 1
rs7034200
GLIS3
1.000 0.080 9 4289050 intron variant C/A;G snv 1