Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2814778
CADM3-AS1 ; ACKR1
0.763 0.360 1 159204893 5 prime UTR variant T/C snv 0.25 11
rs4149056
SLCO1B1
0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 7
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 5
rs116855232
NUDT15
0.742 0.400 13 48045719 missense variant C/T snv 2.8E-02 1.1E-02 4
rs117829974 1.000 0.040 3 62886233 intergenic variant C/A;G;T snv 2
rs2501846 1.000 0.040 1 212668592 upstream gene variant T/C snv 0.24 2
rs2072671
CDA
0.752 0.280 1 20589208 missense variant A/C snv 0.28 0.25 2
rs79206939
FTO
0.925 0.160 16 53826140 missense variant G/A snv 2.1E-03 6.4E-04 2
rs1127354
ITPA
0.667 0.400 20 3213196 missense variant C/A;G snv 7.5E-02 2
rs117506642
LOC105376755
1.000 0.040 2 195143585 intergenic variant C/A;T snv 2
rs776746
CYP3A5 ; ZSCAN25
0.724 0.400 7 99672916 splice acceptor variant T/C snv 0.72 1
rs11141915
DAPK1
0.882 0.160 9 87620879 intron variant A/C snv 0.25 1
rs1801265
DPYD
0.763 0.280 1 97883329 missense variant A/G snv 0.28 1
rs2067079
GAS5 ; SNORA103 ; SNORD80 ; SNORD77 ; SNORD81 ; SNORD44 ; SNORD78 ; SNORD47 ; SNORD79
0.807 0.240 1 173866073 non coding transcript exon variant C/T snv 0.22 0.18 1
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 1
rs2916733
MCPH1
0.851 0.120 8 6465757 intron variant G/A snv 0.28 1
rs2305482
PSMD3
0.851 0.200 17 39984674 intron variant A/C snv 0.57 1
rs149104283
SLCO1B3-SLCO1B7
0.882 0.040 12 20930928 intron variant C/G;T snv 1
rs1142345
TPMT
0.776 0.280 6 18130687 missense variant T/C;G snv 3.7E-02 1