Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs1126407
LOC107985367 ; LGALS8
0.925 0.200 1 236537507 missense variant T/A snv 0.61 0.61 3
rs2737713
LGALS8 ; LOC107985367
1.000 0.120 1 236537507 missense variant T/A snv 2
rs6679356
IL12RB2
0.925 0.200 1 67354511 intron variant C/T snv 0.75 2
rs3753381
SLAMF1
1.000 0.120 1 160629620 intron variant G/A snv 0.31 1
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 44
rs11558538
LOC107985948 ; HNMT
0.695 0.400 2 138002079 missense variant C/T snv 1.0E-01 8.4E-02 19
rs733618
CTLA4
0.763 0.440 2 203866221 upstream gene variant T/C snv 0.10 12
rs16862847
CHRNA1
1.000 0.120 2 174764872 intron variant T/C snv 0.14 1
rs231770 1.000 0.120 2 203864430 upstream gene variant C/T snv 0.42 1
rs564353179
TTN ; LOC101927055
1.000 0.120 2 178780121 missense variant C/G snv 9.6E-05 9.1E-05 1
rs1801394
FASTKD3 ; MTRR
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs4958881
TNIP1
0.827 0.280 5 151070675 intron variant T/C snv 0.21 7
rs3792783
TNIP1
0.882 0.280 5 151076171 intron variant A/G snv 0.25 3
rs1422673
TNIP1
0.925 0.160 5 151059427 intron variant C/G;T snv 2
rs2233287
TNIP1
0.925 0.160 5 151060536 intron variant G/A snv 0.11 2
rs12653117
SEMA5A
1.000 0.120 5 9386473 intron variant C/T snv 0.14 1
rs17209237
NR3C1
1.000 0.120 5 143277647 downstream gene variant A/G snv 0.18 1
rs3792785
TNIP1
1.000 0.120 5 151072089 intron variant T/C snv 0.13 1
rs2187668
LOC107986589 ; HLA-DQA2 ; HLA-DQA1
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 20
rs8321
ZNRD1
0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 16
rs2855812
MICB
0.790 0.360 6 31504943 intron variant G/T snv 0.23 13
rs3099844
MICB-DT
0.732 0.400 6 31481199 non coding transcript exon variant C/A snv 0.11 13