Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10008032
LOC105374413
1.000 0.080 4 38743861 intergenic variant T/C snv 0.66 2
rs10021288 1.000 0.080 4 122084379 downstream gene variant G/A snv 0.21 1
rs10036748
TNIP1
0.752 0.360 5 151078585 intron variant C/A;T snv 11
rs10044254
FBXL7
0.925 0.080 5 15783487 intron variant A/G snv 0.25 2
rs10045431 0.851 0.240 5 159387525 intron variant A/C snv 0.78 4
rs10048897
LINC00528
1.000 0.080 22 17777938 non coding transcript exon variant T/C snv 9.9E-02 1
rs10056243 1.000 0.080 5 110923378 intergenic variant G/A snv 8.0E-02 1
rs10056340 0.925 0.080 5 110854353 intergenic variant T/G snv 0.31 3
rs10074523
KIF3A
1.000 0.080 5 132724891 intron variant C/A snv 0.62 2
rs1007654
GSDMA
1.000 0.080 17 39955101 intron variant A/G snv 0.69 1
rs1008723
GSDMB
0.925 0.160 17 39910014 intron variant G/C;T snv 3
rs1012307
LINC01931 ; MMADHC-DT
1.000 0.080 2 149798707 intron variant A/C snv 4.9E-02 1
rs10131490
RAD51B
1.000 0.080 14 68276590 intron variant A/G;T snv 1
rs10142119 1.000 0.080 14 98020208 intergenic variant G/A;C snv 1
rs10152595
SMAD3
1.000 0.080 15 67183150 intron variant C/G;T snv 2
rs10158467 0.925 0.080 1 173162354 regulatory region variant A/G;T snv 2
rs10173081
IL1RL1 ; IL18R1
1.000 0.080 2 102340888 intron variant C/T snv 0.18 2
rs1017494 1.000 0.080 2 234770601 regulatory region variant C/A;G;T snv 2
rs10174949
LINC00299
1.000 0.080 2 8302118 non coding transcript exon variant G/A snv 0.23 2
rs10178845
LINC00299
1.000 0.080 2 8303673 intron variant G/A snv 0.23 2
rs10187276 0.925 0.080 2 227805721 upstream gene variant T/C snv 0.62 2
rs10189629 1.000 0.080 2 102263004 regulatory region variant C/A snv 0.15 2
rs10192157
IL18R1 ; IL1RL1
1.000 0.080 2 102351896 missense variant C/T snv 0.34 0.46 2
rs10197862
IL18R1 ; IL1RL1
0.925 0.120 2 102350089 intron variant A/G snv 0.18 3
rs10204137
IL18R1 ; IL1RL1
0.925 0.160 2 102351752 missense variant A/G;T snv 0.34 2