Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs111945767 1.000 0.120 6 32549268 downstream gene variant G/C snv 0.45 1
rs11229
PRRC2A
0.851 0.280 6 31635993 synonymous variant A/G snv 0.14 0.17 6
rs1126407
LOC107985367 ; LGALS8
0.925 0.200 1 236537507 missense variant T/A snv 0.61 0.61 3
rs11466316
TGFB1
1.000 0.120 19 41353431 5 prime UTR variant G/A;T snv 1
rs11558538
LOC107985948 ; HNMT
0.695 0.400 2 138002079 missense variant C/T snv 1.0E-01 8.4E-02 19
rs11575936
IFNGR1
0.851 0.200 6 137219288 missense variant C/T snv 1.3E-03 4.1E-04 4
rs1235162
GABBR1
0.827 0.280 6 29569447 intron variant A/G snv 6.0E-02 6
rs1265159
POU5F1
0.882 0.240 6 31172270 intron variant G/A snv 0.21 3
rs12653117
SEMA5A
1.000 0.120 5 9386473 intron variant C/T snv 0.14 1
rs1270942
CFB ; CYP21A2
0.742 0.440 6 31951083 non coding transcript exon variant A/G snv 7.5E-02 11
rs1422673
TNIP1
0.925 0.160 5 151059427 intron variant C/G;T snv 2
rs150881176
HLA-A
1.000 0.120 6 29979963 downstream gene variant T/C snv 1
rs1569686
DNMT3B
0.752 0.400 20 32779273 intron variant G/A;C;T snv 15
rs1634718
MUC22
0.925 0.160 6 31005088 regulatory region variant A/G snv 0.20 3
rs16862847
CHRNA1
1.000 0.120 2 174764872 intron variant T/C snv 0.14 1
rs17209237
NR3C1
1.000 0.120 5 143277647 downstream gene variant A/G snv 0.18 1
rs1794282 0.807 0.320 6 32698749 intergenic variant C/T snv 6.4E-02 6
rs1801275
IL4R
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58
rs1801394
FASTKD3 ; MTRR
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs1805010
IL4R
0.752 0.400 16 27344882 missense variant A/C;G;T snv 0.45 12
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs1980493
BTNL2 ; TSBP1-AS1
0.776 0.400 6 32395438 intron variant T/C snv 0.13 10
rs204990
GPSM3
0.851 0.280 6 32193653 intron variant C/A;T snv 4
rs2071591
ATP6V1G2-DDX39B ; ATP6V1G2 ; NFKBIL1
0.925 0.160 6 31548022 intron variant G/A;C snv 2
rs2187668
LOC107986589 ; HLA-DQA2 ; HLA-DQA1
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 20