Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1010273
PRDM1 ; ATG5
0.882 0.120 6 106107150 synonymous variant G/A snv 9.7E-02 7.7E-02 3
rs10168266
STAT4
0.776 0.400 2 191071078 intron variant C/T snv 0.19 8
rs10204525
PDCD1
0.701 0.440 2 241850169 3 prime UTR variant C/T snv 0.21 20
rs10214910
HLA-DPA1
1.000 0.080 6 33069898 intron variant C/A snv 0.23 0.32 1
rs10243492 1.000 0.080 7 32780825 intergenic variant A/G snv 0.48 1
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs10272859
CDK14
0.925 0.120 7 90689160 intron variant G/C snv 0.39 4
rs1042169
HLA-DPA1 ; HLA-DPB1
1.000 0.080 6 33080909 missense variant G/A;T snv 0.31; 1.4E-02 1
rs1042190
HLA-DPA1
1.000 0.080 6 33069222 missense variant T/C snv 0.24 0.28 1
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1042544
HLA-DPB1
0.925 0.200 6 33086680 3 prime UTR variant A/G snv 0.38 2
rs1046282
ERCC1 ; CD3EAP ; PPP1R13L
0.776 0.160 19 45407414 3 prime UTR variant A/G snv 0.30 10
rs10484569 1.000 0.080 6 33091175 downstream gene variant G/A snv 5.9E-02 1
rs10485138
ASCC3
1.000 0.080 6 100690714 intron variant C/T snv 2.5E-02 1
rs1049334
CAV1
0.851 0.280 7 116560326 3 prime UTR variant G/A;T snv 6
rs1049606
CCND2-AS1 ; CCND2
0.851 0.160 12 4273870 5 prime UTR variant C/T snv 0.58 4
rs1053004
STAT3
0.776 0.280 17 42314074 3 prime UTR variant G/A snv 0.48 11
rs1053005
STAT3
0.763 0.360 17 42313892 3 prime UTR variant T/C snv 0.25 10
rs1054690270
LOC101928953 ; GPT
0.827 0.160 8 144505907 frameshift variant CT/- delins 5
rs1076064
PPARGC1B ; MIR378A
0.851 0.160 5 149732603 intron variant A/G snv 0.47 4
rs10774671
OAS1
0.732 0.480 12 112919388 splice acceptor variant G/A;C snv 0.67 14
rs10853728 0.851 0.160 19 39254506 downstream gene variant C/A;G;T snv 5
rs10912564
TNFSF4
1.000 0.080 1 173201479 intron variant C/T snv 0.43 1
rs10918706
CD247
0.925 0.200 1 167496884 intron variant C/T snv 0.24 2
rs10932029
ICOS ; LOC101927840
0.827 0.200 2 203937045 intron variant T/A;C snv 5