Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7575840 1.000 0.040 2 21050618 intergenic variant G/T snv 0.26 3
rs929596
UGT1A5 ; UGT1A4 ; UGT1A9 ; UGT1A10 ; UGT1A8 ; UGT1A7 ; UGT1A6 ; UGT1A3 ; UGT1A1
0.925 0.040 2 233765830 intron variant A/G snv 0.32 3
rs11887534
ABCG5 ; ABCG8
0.653 0.440 2 43839108 missense variant G/A;C snv 6.4E-06; 6.7E-02 2
rs12988520
UGT1A6 ; UGT1A9 ; UGT1A8 ; UGT1A10 ; UGT1A7
1.000 0.040 2 233698748 intron variant A/C snv 0.51 2
rs2293571
GCKR
0.882 0.120 2 27506613 non coding transcript exon variant G/A snv 0.40 0.39 2
rs2361502
MROH2A
1.000 0.040 2 233790144 intron variant T/C snv 0.30 2
rs569805
ABCB11
1.000 0.040 2 168926370 intron variant A/T snv 0.73 2
rs6711016 1.000 0.040 2 20923592 intergenic variant C/A snv 0.19 2
rs8179252
GCKR
0.882 0.120 2 27523965 downstream gene variant A/C snv 0.37 2
rs7578326
LOC646736
0.882 0.080 2 226155937 TF binding site variant A/G snv 0.36 1
rs782590
PPP4R3B ; LOC107985885
1.000 0.040 2 55616277 intron variant C/T snv 0.44 1
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 4
rs4402960
IGF2BP2
0.724 0.400 3 185793899 intron variant G/T snv 0.38 4
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 1
rs7612463
UBE2E2
0.925 0.080 3 23294959 intron variant C/A;G snv 1
rs900400
LINC02029
0.925 0.080 3 157080986 upstream gene variant T/C snv 0.36 1
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 5
rs11722228
SLC2A9
0.851 0.160 4 9914117 intron variant C/T snv 0.32 4
rs16890979
SLC2A9
0.827 0.200 4 9920543 missense variant C/T snv 0.24 0.29 4
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 3
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 3
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 14
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 10
rs3099844
MICB-DT
0.732 0.400 6 31481199 non coding transcript exon variant C/A snv 0.11 9
rs9465871
CDKAL1
0.882 0.120 6 20717024 intron variant T/C snv 0.30 3