Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12296850 0.925 0.080 12 100426307 downstream gene variant A/G snv 8.7E-02 2
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 2
rs199475643
PAH
0.882 0.240 12 102894894 missense variant T/C snv 8.0E-06 1
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 1
rs121434592
AKT1
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 2
rs314276
LIN28B
0.807 0.280 6 104960124 intron variant A/C snv 0.65 2
rs9657904
CBLB ; LOC107986109
0.925 0.160 3 105867870 intron variant T/A;C snv 1
rs1878022
CMKLR1
0.851 0.080 12 108305255 intron variant C/T snv 0.70 1
rs11080466
PIEZO2
1.000 0.080 18 10899030 intron variant A/G snv 0.31 1
rs17152930
XKR6
1.000 0.080 8 11153316 intron variant G/A snv 4.9E-02 1
rs5744256
IL18
0.827 0.120 11 112152125 intron variant A/G snv 0.16 1
rs1834481
IL18
0.882 0.160 11 112153104 non coding transcript exon variant C/G snv 0.16 2
rs12265047
VTI1A
1.000 0.080 10 112728166 intron variant G/A;C snv 1
rs7086803
VTI1A
0.763 0.160 10 112738717 intron variant G/A snv 0.20 4
rs1143634
IL1B
0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 1
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 2
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 1
rs1143623
IL1B
0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24 1
rs12621220 1.000 0.080 2 112840678 non coding transcript exon variant C/T snv 0.24 1
rs10023113
CAMK2D
1.000 0.080 4 113625548 intron variant A/G snv 0.18 1
rs121913255
NRAS
0.667 0.400 1 114713907 missense variant T/A;G snv 19
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv 25
rs121913237
NRAS
0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 12
rs121913250
NRAS
0.683 0.440 1 114716127 missense variant C/A;G;T snv 13
rs121913671
MET
0.882 0.160 7 116783353 missense variant G/A;C snv 3