Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 16
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 9
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 9
rs3791679
EFEMP1 ; LOC112268416
0.925 0.120 2 55869757 intron variant A/G snv 0.20 8
rs2710323
ITIH1
0.851 0.080 3 52781889 intron variant T/C snv 0.49 0.54 7
rs7531118
LOC105378797
1.000 0.080 1 72371556 intron variant T/C snv 0.40 7
rs10195252
COBLL1
0.925 0.080 2 164656581 intron variant T/C snv 0.48 6
rs55872725
FTO
16 53775211 intron variant C/T snv 0.31 6
rs7133378
DNAH10 ; CCDC92
12 123924955 intron variant G/A snv 0.38 6
rs1812175
HHIP-AS1 ; HHIP
4 144653692 intron variant A/G snv 0.79 5
rs2371767
ADAMTS9-AS2
3 64732582 intron variant G/C snv 0.38 5
rs3786897
PEPD
1.000 0.080 19 33402102 intron variant A/G snv 0.45 5
rs395962
LIN28B
6 104949543 intron variant T/G snv 0.72 5
rs4130548
GIPC2 ; DNAJB4
1.000 0.040 1 77998184 intron variant T/C snv 0.25 5
rs633715 1.000 0.080 1 177883445 intron variant T/C snv 0.17 5
rs7141420
NRXN3
1.000 0.080 14 79433111 intron variant C/T snv 0.56 5
rs7801581
HOXA11-AS ; HOXA11
7 27184152 intron variant C/T snv 0.24 5
rs987237
TFAP2B
0.925 0.120 6 50835337 intron variant A/G snv 0.17 5
rs9930333
FTO
0.882 0.120 16 53766065 intron variant T/C;G snv 5
rs10842707 12 26318431 intron variant C/G;T snv 4
rs10923712
TBX15
1 118962811 intron variant G/A snv 0.56 4
rs12429545 13 53528071 intron variant G/A;T snv 0.12 4
rs17024393
GNAT2
1 109612066 intron variant T/C snv 4.6E-02 4
rs1936807
RSPO3
6 127127104 intron variant C/G snv 0.55 4
rs2033529
TDRG1
6 40380914 intron variant A/C;G snv 4