Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10887800
LOC101929727 ; RNLS
0.790 0.280 10 88316086 intron variant A/G;T snv 11
rs7025417
LOC107987046 ; IL33
0.752 0.280 9 6240084 intron variant T/C;G snv 11
rs10507391
ALOX5AP
0.776 0.320 13 30737959 intron variant A/T snv 0.52 10
rs11172113
LRP1
0.882 0.080 12 57133500 intron variant T/C snv 0.42 10
rs1799987
CCR5AS ; CCR5
0.763 0.200 3 46370444 intron variant A/G snv 0.49 10
rs320
LPL
0.827 0.200 8 19961566 intron variant T/A;G snv 9
rs4845625
IL6R
0.851 0.080 1 154449591 intron variant T/C snv 0.60 9
rs880315
CASZ1
0.925 0.120 1 10736809 intron variant T/C snv 0.32 9
rs9797861
SLC44A2
0.790 0.200 19 10632450 intron variant C/A;G;T snv 9
rs1041740
SOD1
0.807 0.320 21 31667849 intron variant C/T snv 0.24 8
rs17228212
SMAD3
0.807 0.160 15 67166301 intron variant T/C snv 0.21 8
rs7136446
IGF1 ; LINC02456
0.882 0.160 12 102444737 intron variant C/T snv 0.66 8
rs9333025
CYP4A11
0.851 0.200 1 46931231 intron variant C/T snv 9.4E-02 8
rs10118757
MTAP
0.827 0.120 9 21853340 intron variant A/G snv 0.26 7
rs10432782
SOD1
0.807 0.160 21 31664078 intron variant T/G snv 0.19 7
rs16867253
GRHL1
0.851 0.120 2 9956965 intron variant G/T snv 5.8E-02 7
rs2359612
VKORC1
0.851 0.120 16 31092475 intron variant A/G snv 0.66 7
rs4444878
F11-AS1
0.851 0.120 4 186292729 intron variant C/A;T snv 7
rs4846914
GALNT2
0.925 0.080 1 230159944 intron variant G/A snv 0.45 6
rs702553
PDE4D
0.882 0.160 5 60440946 intron variant A/T snv 0.37 6
rs7173743
MORF4L1
0.851 0.120 15 78849442 intron variant T/C snv 0.45 6
rs753152
RAMP2-AS1 ; RAMP2
0.882 0.160 17 42761487 intron variant T/G snv 0.12 6
rs9551963
ALOX5AP
0.851 0.160 13 30758410 intron variant A/C;T snv 6
rs9579646
ALOX5AP
0.851 0.160 13 30736442 intron variant G/A;T snv 6
rs9937053
FTO
0.882 0.160 16 53765595 intron variant G/A snv 0.42 6