Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs855791
TMPRSS6
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 8
rs13394720 1.000 2 233593475 intergenic variant T/C snv 7.0E-02 6
rs887829
UGT1A8 ; UGT1A5 ; UGT1A6 ; UGT1A7 ; UGT1A4 ; UGT1A3 ; UGT1A10 ; UGT1A1 ; UGT1A9
0.763 0.280 2 233759924 intron variant C/T snv 0.36 6
rs4149056
SLCO1B1
0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 5
rs11563251
UGT1A9 ; UGT1A7 ; UGT1A3 ; UGT1A6 ; UGT1A5 ; UGT1A1 ; UGT1A4 ; UGT1A10 ; UGT1A8
2 233770738 3 prime UTR variant C/T snv 0.19 5
rs1550532
DGKD
2 233356202 intron variant C/G snv 0.75 4
rs4149081
SLCO1B1
1.000 0.040 12 21225087 intron variant G/A snv 0.18 4
rs11891311
UGT1A8 ; UGT1A3 ; UGT1A5 ; UGT1A9 ; UGT1A10 ; UGT1A4 ; UGT1A6 ; UGT1A7
2 233730664 intron variant G/A snv 0.42 4
rs17864661 2 233587096 downstream gene variant C/T snv 0.14 3
rs2602362 2 233607902 downstream gene variant A/C snv 0.22 3
rs2602363 2 233611879 intergenic variant T/C snv 0.22 3
rs2602364 2 233615583 upstream gene variant G/A snv 0.22 3
rs2741019 2 233602042 upstream gene variant C/A;G snv 3
rs2741021 2 233603237 upstream gene variant C/T snv 0.22 3
rs2741027 1.000 0.040 2 233609365 downstream gene variant G/A snv 0.22 3
rs2741028 2 233610268 intergenic variant G/A;T snv 3
rs11694406
DGKD
2 233423164 intron variant G/A snv 0.12 3
rs6741669
DNAJB3 ; UGT1A8 ; UGT1A9 ; UGT1A7 ; UGT1A3 ; UGT1A6 ; UGT1A10 ; UGT1A5 ; UGT1A4
2 233744546 intron variant A/G snv 0.55 3
rs11045879
SLCO1B1
1.000 0.120 12 21229685 intron variant T/C snv 0.18 3
rs2417940
SLCO1B3 ; SLCO1B3-SLCO1B7
12 20864941 intron variant T/A;C snv 3
rs4148324
UGT1A10 ; UGT1A3 ; UGT1A6 ; UGT1A4 ; UGT1A7 ; UGT1A8 ; UGT1A9 ; UGT1A5 ; UGT1A1
2 233764076 intron variant T/A;G snv 0.36 3
rs6715325
UGT1A10 ; UGT1A7 ; UGT1A8 ; UGT1A6 ; UGT1A9 ; UGT1A5 ; UGT1A4
2 233726595 intron variant T/C snv 0.46 3
rs10175809
UGT1A10 ; UGT1A7 ; UGT1A8 ; UGT1A9
2 233688219 intron variant T/A snv 0.39 3
rs11892031
UGT1A10 ; UGT1A8
0.882 0.120 2 233656637 intron variant A/C;T snv 3
rs2741034
UGT1A10 ; UGT1A8
2 233640168 intron variant A/G snv 0.22 3