Source: GWASDB ×
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 24
rs2247056
LOC112267902 ; HLA-B ; LINC02571
0.882 0.160 6 31297713 intron variant T/C snv 0.80 8
rs185819
TNXB
0.851 0.200 6 32082290 missense variant T/A;C;G snv 8.2E-06; 0.58; 4.1E-06 8
rs2516448 0.827 0.120 6 31422633 intron variant T/C;G snv 7
rs13437082 1.000 6 31386783 upstream gene variant C/T snv 0.32 6
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 6
rs6570507
ADGRG6
0.827 0.240 6 142358435 intron variant G/A snv 0.47 6
rs6457620 0.882 0.200 6 32696222 intergenic variant G/C snv 0.52 4
rs864745
JAZF1
0.763 0.320 7 28140937 intron variant T/C snv 0.41 4
rs2284746
MFAP2
1 16980180 intron variant C/A;G snv 4
rs11891311
UGT1A8 ; UGT1A3 ; UGT1A5 ; UGT1A9 ; UGT1A10 ; UGT1A4 ; UGT1A6 ; UGT1A7
2 233730664 intron variant G/A snv 0.42 4
rs17391694 0.882 0.120 1 78157942 regulatory region variant C/T snv 7.8E-02 3
rs2844479 0.925 0.200 6 31605179 intergenic variant A/C snv 0.34 3
rs6959212 7 38088724 intergenic variant T/C;G snv 3
rs7763064 6 142476152 intergenic variant G/A snv 0.38 3
rs3748069
ADGRG6
6 142446496 downstream gene variant A/G snv 0.39 3
rs4896582
ADGRG6
6 142382740 intron variant G/A snv 0.50 3
rs7741741
ADGRG6
0.925 0.040 6 142334664 intron variant T/A;G snv 3
rs10946808
H2AC9P
1.000 0.040 6 26233159 non coding transcript exon variant A/G snv 0.26 3
rs314277
LIN28B
0.925 0.080 6 104959787 intron variant A/C;G;T snv 3
rs5742915
PML
0.925 0.080 15 74044292 missense variant T/C;G snv 0.35; 4.0E-06 3
rs2417940
SLCO1B3 ; SLCO1B3-SLCO1B7
12 20864941 intron variant T/A;C snv 3
rs11024739
SPTY2D1
11 18624296 intron variant C/A;G snv 3
rs4148323
UGT1A10 ; UGT1A9 ; UGT1A7 ; UGT1A3 ; UGT1A5 ; UGT1A6 ; UGT1A8 ; UGT1A1 ; UGT1A4
0.701 0.440 2 233760498 missense variant G/A snv 2.2E-02 9.2E-03 3
rs1659127 16 14294448 intergenic variant G/A;C;T snv 2