Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs61776719 0.776 0.120 1 37995647 downstream gene variant C/A snv 0.46 11
rs1537372
CDKN2B-AS1
0.752 0.120 9 22103184 intron variant G/A;T snv 11
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 10
rs651821
APOA5
0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 10
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 10
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 10
rs715
CPS1
1.000 0.040 2 210678331 3 prime UTR variant T/C snv 0.28 10
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 10
rs10857147 1.000 0.040 4 80259918 intergenic variant A/T snv 0.25 9
rs459193
C5orf67
0.925 0.120 5 56510924 downstream gene variant A/G snv 0.69 9
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 9
rs7528419
CELSR2
0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 9
rs4919687
CYP17A1
0.742 0.160 10 102835491 non coding transcript exon variant G/A snv 0.25 9
rs3918226
NOS3
0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02 9
rs2107595 0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19 8
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 8
rs604723
ARHGAP42
1.000 0.040 11 100739815 intron variant T/C snv 0.78 8
rs633185
ARHGAP42
0.925 0.080 11 100722807 intron variant G/A;C snv 8
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 8
rs9349379
PHACTR1
0.732 0.200 6 12903725 intron variant A/G snv 0.32 8
rs17293632
SMAD3
0.763 0.240 15 67150258 intron variant C/T snv 0.17 8
rs2571445
TNS1
0.925 0.080 2 217818431 missense variant A/G;T snv 0.62 8
rs887829
UGT1A8 ; UGT1A5 ; UGT1A6 ; UGT1A7 ; UGT1A4 ; UGT1A3 ; UGT1A10 ; UGT1A1 ; UGT1A9
0.763 0.280 2 233759924 intron variant C/T snv 0.36 8
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 7
rs550057
ABO
0.925 0.080 9 133271182 intron variant T/A;C snv 7