Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10036748
TNIP1
0.752 0.360 5 151078585 intron variant C/A;T snv 11
rs1005714
NUP85 ; GGA3
1.000 0.040 17 75228544 5 prime UTR variant G/C snv 0.78 1
rs10168266
STAT4
0.776 0.400 2 191071078 intron variant C/T snv 0.19 8
rs10174238
STAT4
0.724 0.200 2 191108308 intron variant G/A snv 0.70 14
rs10178332
ROCK2
0.925 0.120 2 11268891 intron variant C/A;G snv 2
rs10186029
IKZF2
1.000 0.040 2 213064562 intron variant C/T snv 0.40 1
rs10220668
LINC01500
1.000 0.040 14 59042487 intron variant A/G snv 0.30 1
rs1035798
AGER
1.000 0.040 6 32183445 splice region variant G/A snv 0.24 0.19 1
rs10406069
CD22 ; MIR5196
1.000 0.040 19 35345627 missense variant G/A;C snv 0.16 1
rs10413500
CD22 ; MIR5196
1.000 0.040 19 35345923 intron variant C/G snv 0.16 1
rs10419538
CD22
1.000 0.040 19 35333116 intron variant C/G snv 0.11 1
rs10488631
TNPO3
0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 13
rs10498070 0.925 0.080 2 219833404 intergenic variant A/C snv 0.39 2
rs10499194 0.752 0.400 6 137681500 intron variant C/T snv 0.24 10
rs10499197 0.925 0.080 6 137811379 intergenic variant T/G snv 2.4E-02 2
rs10516487
BANK1
0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 11
rs1059702
IRAK1
0.807 0.280 X 154018741 missense variant A/G snv 0.72 7
rs10744676
KCNA5
0.925 0.080 12 5043783 upstream gene variant C/T snv 0.88 2
rs10865710
PPARG
0.763 0.360 3 12311699 intron variant C/G snv 0.25 13
rs10912580
TNFSF4 ; LOC100506023
0.882 0.080 1 173287411 intergenic variant A/G snv 0.21 3
rs10946216
CCR6
1.000 0.040 6 167125409 intron variant T/C snv 0.61 1
rs10954213
IRF5
0.752 0.200 7 128949373 3 prime UTR variant G/A snv 0.58 11
rs10954214
IRF5
0.851 0.160 7 128949579 3 prime UTR variant C/T snv 0.64 4
rs11047102
SOX5
0.925 0.160 12 23793212 intron variant C/T snv 7.9E-02 2
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 12