Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 9
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 9
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 8
rs9987289
LOC157273
1.000 0.040 8 9325848 non coding transcript exon variant A/G snv 0.87 8
rs4148325
UGT1A8 ; UGT1A5 ; UGT1A10 ; UGT1A7 ; UGT1A1 ; UGT1A9 ; UGT1A3 ; UGT1A4 ; UGT1A6
0.851 0.080 2 233764663 intron variant C/T snv 0.36 8
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 7
rs116843064
ANGPTL4
0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02 7
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 7
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 7
rs174546
FADS1 ; FADS2
0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 7
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 7
rs929596
UGT1A5 ; UGT1A4 ; UGT1A9 ; UGT1A10 ; UGT1A8 ; UGT1A7 ; UGT1A6 ; UGT1A3 ; UGT1A1
0.925 0.040 2 233765830 intron variant A/G snv 0.32 7
rs17863787
UGT1A9 ; UGT1A8 ; UGT1A6 ; UGT1A7 ; UGT1A10
0.925 0.040 2 233702448 intron variant T/G snv 0.30 7
rs6993770
ZFPM2 ; ZFPM2-AS1
0.925 0.080 8 105569300 intron variant A/T snv 0.31 7
rs173539 0.882 0.080 16 56954132 intergenic variant C/T snv 0.33 6
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 6
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24 6
rs2043085
ALDH1A2
0.827 0.080 15 58388755 intron variant T/C snv 0.54 6
rs2266788
APOA5 ; ZPR1
0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93 6
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 6
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 5
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 5
rs12686004
ABCA1
1.000 0.040 9 104891145 intron variant G/A snv 9.1E-02 5
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 5
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 5