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
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs13333226
UMOD
0.827 0.200 16 20354332 intron variant A/G snv 0.23 10
rs4821480
MYH9
0.807 0.160 22 36299201 intron variant G/T snv 0.78 9
rs1041740
SOD1
0.807 0.320 21 31667849 intron variant C/T snv 0.24 8
rs4293393
UMOD
0.827 0.200 16 20353266 intron variant A/G snv 0.20 8
rs1106766
R3HDM2
0.882 0.120 12 57415673 intron variant C/T snv 0.19 7
rs1800783
NOS3
0.827 0.280 7 150992309 intron variant A/C;G;T snv 7
rs6677604
CFH
0.827 0.200 1 196717788 intron variant G/A snv 0.23 7
rs17883901
GCLC
0.851 0.240 6 53545239 intron variant G/A;T snv 6.2E-02 6
rs2237897
KCNQ1
0.882 0.200 11 2837316 intron variant C/T snv 8.1E-02 6
rs2268388
ACACB
0.851 0.200 12 109205840 intron variant G/A snv 0.14 6
rs6495446
MTHFS ; ST20-MTHFS
0.851 0.200 15 79862640 intron variant C/T snv 0.31 6
rs702553
PDE4D
0.882 0.160 5 60440946 intron variant A/T snv 0.37 6
rs11089788
MYH9
0.851 0.120 22 36355056 intron variant C/A snv 0.46 5
rs2412971
HORMAD2
0.882 0.320 22 30098382 intron variant G/A snv 0.55 5
rs2248098
VDR
0.925 0.120 12 47859573 intron variant A/G;T snv 4
rs841853
SLC2A1
0.882 0.200 1 42935767 intron variant A/C snv 0.66 4
rs12449782 0.925 0.200 17 63498888 intron variant G/A snv 0.41 3
rs136161
APOL1
0.925 0.160 22 36261386 intron variant G/C snv 0.51 3
rs2281999
UNC13B
0.925 0.160 9 35381507 intron variant C/T snv 0.35 0.38 3
rs2607420
ITPKC
0.925 0.120 19 40738982 intron variant G/A snv 0.76 3
rs741301
ELMO1
0.925 0.160 7 36878390 intron variant C/T snv 0.59 3