Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13437088 0.925 0.040 6 31387342 intergenic variant C/T snv 0.32 6
rs1062470
PSORS1C1 ; CDSN
0.925 0.040 6 31116658 synonymous variant G/A snv 0.37 0.41 5
rs9468925
HLA-B
0.851 0.040 6 31291060 intron variant G/A snv 0.44 5
rs11652075
CARD14 ; SGSH
0.882 0.040 17 80205094 missense variant C/T snv 0.41 0.40 3
rs2778031 1.000 0.040 9 88220811 intergenic variant T/A;C snv 3
rs9266150
MIR6891 ; HLA-B
0.925 0.040 6 31356368 missense variant A/C;G;T snv 0.12; 7.9E-05; 3.8E-04 3
rs9504361
EXOC2
1.000 0.040 6 577820 intron variant A/G snv 0.40 3
rs1020760
NFKB1
0.925 0.040 4 102593288 non coding transcript exon variant C/G snv 0.42 2
rs1056198
RNF114
0.925 0.040 20 49939692 intron variant C/T snv 0.34 2
rs10782001
FBXL19
1.000 0.040 16 30931304 intron variant G/A snv 0.53 2
rs10789285 1.000 0.040 1 69322799 intergenic variant T/G snv 0.33 2
rs11593576
ZMIZ1
0.925 0.040 10 79256139 intron variant C/T snv 0.29 2
rs12445568
STX1B
0.925 0.040 16 30993491 splice region variant T/C snv 0.39 0.38 2
rs12602912
BPTF
1.000 0.040 17 67873957 intron variant C/G;T snv 2
rs1265181
PSORS1C3
0.925 0.040 6 31188008 intergenic variant G/C snv 0.15 2
rs12884468 0.925 0.040 14 35383280 downstream gene variant T/C snv 0.47 2
rs13708
STX1B ; HSD3B7
1.000 0.040 16 30989488 3 prime UTR variant G/A;C snv 0.52 2
rs1473247
RNF145
1.000 0.040 5 159176563 intron variant T/C snv 0.41 2
rs1713239
IL20
1.000 0.040 1 206864130 upstream gene variant G/C snv 0.88 2
rs17716942
KCNH7
0.925 0.040 2 162404181 intron variant T/C snv 9.6E-02 2
rs201909740
CD28
1.000 0.040 2 203734889 missense variant G/A snv 4.0E-06 1.4E-05 2
rs2066819
STAT2
0.925 0.040 12 56356420 intron variant C/T snv 4.9E-02 4.5E-02 2
rs2233278
TNIP1
0.925 0.040 5 151087628 5 prime UTR variant G/C;T snv 4.8E-02 2
rs2675662
CAMK2G
0.925 0.040 10 73839369 intron variant A/G snv 0.55 2
rs27432
ERAP1 ; LOC102724748
0.925 0.040 5 96783569 intron variant A/C;G snv 2