Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs669661
PRG3
11 57380702 missense variant A/G snv 0.99 0.96 1
rs222826 0.851 0.120 2 146120964 regulatory region variant T/C snv 0.94 16
rs7190256
ZFHX3
0.851 0.120 16 72963084 intron variant C/T snv 0.94 16
rs783396
CRYBG1
1.000 0.080 6 106539495 missense variant A/C snv 0.93 0.93 2
rs9465922
CDKAL1
6 20865366 intron variant C/A snv 0.92 1
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs1492099
AGTR1
0.882 0.120 3 148719716 intron variant T/A;C snv 0.89 5
rs229961 5 57690889 regulatory region variant T/C snv 0.87 1
rs4795895
CCL11
1.000 0.120 17 34284427 upstream gene variant A/G snv 0.86 2
rs10033464 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 8
rs2632512
TSPOAP1-AS1 ; RNF43
17 58374461 intron variant T/C snv 0.85 1
rs822391
ADIPOQ
0.925 0.080 3 186846014 intron variant C/T snv 0.85 4
rs2867125 0.925 0.120 2 622827 intergenic variant T/A;C snv 0.85 8
rs2288904
SLC44A2
0.807 0.240 19 10631494 missense variant A/G snv 0.80 0.83 8
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs9604365 13 111922883 intergenic variant G/A snv 0.82 1
rs822396
ADIPOQ
0.732 0.400 3 186849088 intron variant G/A snv 0.81 16
rs650439
KL
1.000 0.080 13 33061802 intron variant T/A snv 0.82 0.81 3
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 28
rs2986017
CALHM1
0.851 0.120 10 103458495 missense variant A/G snv 0.79 0.80 6
rs261332
ALDH1A2 ; LIPC-AS1 ; LIPC
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 20
rs2132572
IGFBP3
1.000 7 45921946 upstream gene variant T/C snv 0.79 3
rs1051931
PLA2G7
0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19
rs2794521
CRP
0.742 0.480 1 159715306 upstream gene variant C/T snv 0.78 15
rs504615 6 44627475 regulatory region variant G/A snv 0.78 1