Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 28
rs708272
CETP
0.708 0.440 16 56962376 intron variant G/A snv 0.42 0.38 24
rs7120118
NR1H3
0.716 0.360 11 47264739 intron variant T/C snv 0.38 18
rs1800588
ALDH1A2 ; LIPC
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 16
rs2070895
LIPC ; ALDH1A2
0.807 0.120 15 58431740 intron variant G/A snv 0.33 15
rs4580704
CLOCK
0.790 0.200 4 55460540 intron variant G/C snv 0.69 13
rs17465637
MIA3
0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 11
rs780092
GCKR
0.827 0.160 2 27520287 intron variant A/G snv 0.18 10
rs2074192
ACE2
0.827 0.160 X 15564667 intron variant C/T snv 0.40 9
rs4845625
IL6R
0.851 0.080 1 154449591 intron variant T/C snv 0.60 9
rs5030717
TLR4
0.807 0.240 9 117711556 intron variant A/G snv 0.13 9
rs1984112
CD36
0.807 0.280 7 80613604 intron variant A/G snv 0.33 8
rs2106809
ACE2
0.827 0.120 X 15599938 intron variant A/G snv 0.19 8
rs4773144
COL4A1 ; COL4A2
0.827 0.080 13 110308365 intron variant A/G snv 0.42 7
rs6922269
MTHFD1L
0.807 0.200 6 150931849 intron variant G/A snv 0.35 7
rs1799884
GCK
1.000 0.080 7 44189469 intron variant C/T snv 0.17 6
rs805297
BAG6 ; APOM
0.851 0.280 6 31654829 intron variant C/A snv 0.23 6
rs2281997
ENHO
0.882 0.240 9 34521869 intron variant T/A;C snv 5
rs2292318
SLC12A4
0.925 0.120 16 67951803 intron variant C/A;T snv 0.15 5
rs4363657
SLCO1B1
12 21215788 intron variant T/C snv 0.18 5