Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs12759054
SLC35F3
1.000 0.040 1 233984064 intron variant T/A;C snv 3
rs80274284
SLC22A15
1 116037356 missense variant G/T snv 1
rs200655768
TTN-AS1 ; TTN
2 178711222 synonymous variant G/A;T snv 1
rs6797827 3 109735523 intron variant C/T snv 0.18 1
rs116671518
DKK2
4 107189709 intron variant T/C snv 1.9E-02 1
rs5861895 4 129344228 regulatory region variant TT/-;T;TTT delins 1
rs62309385 4 136134743 intron variant G/C snv 9.8E-02 1
rs2395185
HLA-DRB9
0.724 0.360 6 32465390 intron variant G/T snv 0.29 17
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 13
rs2516049
HLA-DRB1
0.742 0.400 6 32602623 intergenic variant T/C snv 0.27 12
rs477515
HLA-DRB1
0.790 0.400 6 32601914 intergenic variant G/A snv 0.27 10
rs652888
EHMT2-AS1 ; EHMT2 ; LOC107986588 ; CYP21A2
0.776 0.480 6 31883457 non coding transcript exon variant A/G snv 0.18 0.20 10
rs9268853
HLA-DRB9
0.790 0.440 6 32461866 intron variant T/C snv 0.29 10
rs3115663
PRRC2A ; MIR6832
0.827 0.360 6 31634066 non coding transcript exon variant T/C snv 0.17 7
rs3130618
CSNK2B ; GPANK1
0.827 0.360 6 31664357 missense variant C/A;T snv 0.15; 4.0E-06 7
rs7192
HLA-DRA
0.827 0.200 6 32443869 missense variant T/G snv 0.64 0.61 7
rs7194
HLA-DRA
0.827 0.280 6 32444703 3 prime UTR variant G/A snv 0.61 7
rs11229
PRRC2A
0.851 0.280 6 31635993 synonymous variant A/G snv 0.14 0.17 6
rs2239804
HLA-DRA
0.851 0.240 6 32443746 intron variant T/A;C snv 0.51 5
rs2395182
HLA-DRA
0.851 0.280 6 32445540 downstream gene variant G/T snv 0.76 5
rs10947261
BTNL2 ; TSBP1-AS1
0.882 0.240 6 32405455 splice region variant G/T snv 0.11 4
rs204994
PBX2
0.925 0.120 6 32187221 non coding transcript exon variant C/T snv 0.18 0.21 4
rs2227139 0.925 0.160 6 32445682 downstream gene variant G/A snv 0.61 4
rs2239802
HLA-DRA
0.882 0.200 6 32444069 intron variant C/A;G;T snv 4