Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs41423247
NR3C1
0.695 0.440 5 143399010 intron variant G/C snv 0.31 23
rs2072472
IL1R2
0.732 0.200 2 102026557 intron variant A/G snv 0.24 13
rs33388
NR3C1
0.776 0.360 5 143317730 intron variant A/T snv 0.53 12
rs11896604
ACYP2
0.776 0.200 2 54252062 intron variant C/A;G;T snv 8
rs17045754
LOC105374610 ; ACYP2
0.790 0.280 2 54269620 intron variant G/A;C snv 7
rs4851527
IL1R2
0.790 0.160 2 102005914 intron variant A/G snv 0.63 7
rs719250
IL1R2
0.827 0.200 2 102007256 intron variant C/T snv 0.11 5
rs12615793
ACYP2
0.851 0.280 2 54248777 intron variant G/A;T snv 4
rs480902
EGLN1
0.882 0.200 1 231395881 intron variant T/C snv 0.64 3
rs6089953
RTEL1-TNFRSF6B ; RTEL1
0.882 0.080 20 63659655 intron variant A/G snv 0.82 3
rs72625676
GALNT16
0.882 0.120 14 69307268 intron variant C/T snv 6.3E-02 3
rs130293
SYN3 ; TIMP3
1.000 0.040 22 32825953 intron variant G/A snv 0.92 1
rs157928
LINC-PINT ; LINC00513
1.000 0.040 7 130896599 intron variant T/C snv 0.29 1
rs2918417
NR3C1
1.000 0.040 5 143346605 intron variant C/T snv 0.29 1
rs4461142 1.000 0.040 17 63500687 intron variant T/C snv 0.62 1
rs4634384
NR3C1
1.000 0.040 5 143401132 intron variant C/T snv 0.52 1
rs4963516
P3H3
1.000 0.040 12 6838864 intron variant T/G snv 0.15 1
rs6010621
RTEL1-TNFRSF6B ; RTEL1
1.000 0.040 20 63679519 intron variant T/G snv 0.81 1
rs6188
NR3C1
1.000 0.040 5 143300779 intron variant C/A snv 0.26 0.29 1
rs749174
GSTP1
1.000 0.040 11 67585782 intron variant G/A snv 0.29 1
rs8066114
ACE3P
1.000 0.040 17 63512479 intron variant C/G snv 0.36 1
rs843752
ACYP2
1.000 0.040 2 54219450 intron variant T/A;G snv 1
rs199983 1.000 0.040 6 104412396 intergenic variant A/G snv 0.52 1
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246