Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4072037
MUC1
0.732 0.240 1 155192276 splice acceptor variant C/A;T snv 0.59 4
rs1481012
ABCG2
0.882 0.200 4 88117930 intron variant A/G snv 8.9E-02 3
rs2622621
ABCG2
0.851 0.240 4 88109768 intron variant C/A;G snv 3
rs8176746
ABO
0.882 0.160 9 133255935 missense variant G/A;T snv 4.1E-06; 0.12 3
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 3
rs7014346
CASC8 ; POU5F1B ; PCAT1
0.732 0.240 8 127412547 intron variant A/G snv 0.63 3
rs7754840
CDKAL1
0.807 0.200 6 20661019 intron variant G/A;C;T snv 3
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 3
rs2274910
ITLN1
0.827 0.200 1 160882256 non coding transcript exon variant T/C snv 0.65 0.58 3
rs314277
LIN28B
0.925 0.080 6 104959787 intron variant A/C;G;T snv 3
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 3
rs6983267
PCAT1 ; CCAT2 ; CASC8 ; POU5F1B
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 3
rs2274223
PLCE1
0.620 0.400 10 94306584 missense variant A/G snv 0.28 0.31 3
rs2294008
PSCA ; JRK
0.672 0.320 8 142680513 5 prime UTR variant C/T snv 0.46 0.45 3
rs12255372
TCF7L2
0.667 0.480 10 113049143 intron variant G/A;T 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
rs2070959
UGT1A8 ; UGT1A7 ; UGT1A9 ; UGT1A10 ; UGT1A6
0.742 0.320 2 233693545 missense variant A/G snv 0.31 0.30 3
rs11676348 0.790 0.160 2 218145423 regulatory region variant C/G;T snv 2
rs12413624 0.851 0.120 10 118519432 intergenic variant T/A snv 0.34 2
rs16892766 0.716 0.240 8 116618444 intergenic variant A/C snv 9.3E-02 2
rs4242382 0.763 0.240 8 127505328 intergenic variant A/G;T snv 2
rs4444235 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 2
rs4779584 0.732 0.160 15 32702555 intergenic variant T/C snv 0.67 2
rs6687758 0.763 0.200 1 221991606 regulatory region variant A/G snv 0.20 2
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 2