Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 35
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 23
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 23
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 16
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 13
rs174594
FADS2
0.776 0.160 11 61852357 intron variant C/A;T snv 13
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 12
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 9
rs10774625
ATXN2
0.763 0.320 12 111472415 intron variant A/G snv 0.66 7
rs77924615
PDILT
1.000 0.080 16 20381010 intron variant G/A snv 0.16 7
rs12423664
FBRSL1
1.000 0.040 12 132493308 intron variant G/A snv 0.10 6
rs2244608
HNF1A ; HNF1A-AS1
0.882 0.160 12 120979185 intron variant A/G snv 0.29 6
rs11072567
NRG4
15 76006403 intron variant A/G snv 0.43 5
rs1481012
ABCG2
0.882 0.200 4 88117930 intron variant A/G snv 8.9E-02 5
rs4148155
ABCG2
0.882 0.200 4 88133515 intron variant A/G snv 8.7E-02 5
rs62033406
FTO
16 53790314 intron variant A/G snv 0.33 5
rs79598313
KDF1
1 26958422 intron variant C/A;T snv 5
rs11204682
ENSA
1 150623061 intron variant G/A;T snv 4
rs1171616
SLC16A9
0.882 0.200 10 59708831 intron variant G/T snv 0.79 4
rs12801636
PCNX3
1.000 0.040 11 65623846 intron variant G/A snv 0.25 4
rs13129697
SLC2A9
0.925 0.120 4 9925343 intron variant T/G snv 0.39 4
rs1394125
UBE2Q2
0.882 0.200 15 75866642 intron variant G/A;T snv 4
rs1407040
GNAS
20 58897119 intron variant C/T snv 0.70 4
rs187355703
HOXD-AS2 ; LOC100129455 ; HOXD8
1.000 0.080 2 176128855 intron variant C/G snv 1.5E-02 1.5E-02 4
rs4766566
CUX2
0.851 0.200 12 111269073 intron variant C/T snv 0.42 4