Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs998731
TPD52 ; LOC105375920
1.000 0.120 8 80183160 intron variant C/G;T snv 1
rs9979383
RUNX1
0.925 0.200 21 35343463 intron variant C/G;T snv 5
rs991760
TAP1 ; PSMB9
1.000 0.120 6 32855790 intron variant G/A snv 8.2E-02 1
rs9909240
LOC105371532 ; NTN1
1.000 0.120 17 9236774 intron variant G/A snv 0.50 1
rs9880772 0.827 0.240 3 27736288 intergenic variant G/A snv 0.59 5
rs987870
HLA-DPA1 ; HLA-DPB1
0.851 0.160 6 33075103 intron variant A/G snv 0.19 4
rs986521
COL11A2
1.000 0.120 6 33168368 intron variant G/A;C snv 1
rs9860428 1.000 0.120 3 112852072 intergenic variant C/A;G;T snv 1
rs984778 1.000 0.120 6 32432311 TF binding site variant C/T snv 0.62 1
rs983561 1.000 0.120 6 32435878 upstream gene variant T/C;G snv 1
rs9826828
STAG1
1.000 0.120 3 136683218 intron variant G/A snv 1.3E-02 1
rs9785133 1.000 0.120 8 20501107 intergenic variant C/T snv 0.21 1
rs9784876 1.000 0.120 6 32821101 intron variant C/A snv 0.11 1
rs9784858
HLA-DOB
0.925 0.200 6 32819398 intron variant G/C snv 0.12 2
rs9784758 0.925 0.200 6 32820734 intron variant T/C snv 0.11 2
rs9770242
NAMPT
0.851 0.240 7 106285885 5 prime UTR variant C/A snv 0.79 5
rs969891
TSBP1 ; TSBP1-AS1
1.000 0.120 6 32348638 intron variant T/C;G snv 1
rs969129
LOC105374724 ; IL7R
0.851 0.200 5 35861166 intron variant T/A;G snv 4
rs968567
FADS2 ; FADS1
0.851 0.240 11 61828092 intron variant C/T snv 0.11 7
rs9653442
LINC01104
1.000 0.120 2 100208905 intron variant C/T snv 0.46 2
rs9651713
CASP5
1.000 0.120 11 105004030 intron variant G/A snv 0.13 1
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs9635
TCP11L1 ; LINC00294 ; CSTF3
1.000 0.120 11 33079306 non coding transcript exon variant C/T snv 1
rs9610
IL10RA ; SMIM35
0.882 0.240 11 118001371 3 prime UTR variant G/A;T snv 0.51 4
rs9604529
LINC00452
1.000 0.120 13 113919624 non coding transcript exon variant A/G;T snv 0.17; 7.4E-06 1