Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 11
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 11
rs687621
ABO
0.851 0.240 9 133261662 intron variant G/A;C snv 11
rs6983267
PCAT1 ; CCAT2 ; CASC8 ; POU5F1B
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 11
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 11
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 10
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 10
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 10
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 10
rs6857
NECTIN2
0.790 0.240 19 44888997 3 prime UTR variant C/T snv 0.13 10
rs2735940
TERT
0.689 0.400 5 1296371 upstream gene variant A/G snv 0.49 10
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 9
rs459193
C5orf67
0.925 0.120 5 56510924 downstream gene variant A/G snv 0.69 9
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 9
rs1128249
COBLL1
1.000 0.080 2 164672114 intron variant G/C;T snv 9
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 9
rs1800437
GIPR
0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 9
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
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 9
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 8
rs2820443 0.882 0.120 1 219580167 regulatory region variant T/C snv 0.23 8
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 8
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 8
rs10224002
PRKAG2
0.925 0.080 7 151717955 intron variant A/G snv 0.31 8