Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs370711144
IL16
1.000 15 81225649 missense variant G/A;T snv 2.7E-04 1
rs2292399
PPDPFL
1.000 8 49074671 3 prime UTR variant A/G snv 0.31 1
rs7514229
TNFSF4
1.000 1 173185165 3 prime UTR variant G/T snv 0.43 1
rs2618431
FAM167A
0.925 0.120 8 11466955 intron variant A/G snv 0.87 2
rs2227478
IL22 ; LOC105369818
0.925 0.040 12 68254842 upstream gene variant A/G snv 0.37 2
rs2069550
TG
0.925 0.120 8 132888141 synonymous variant T/C snv 0.58 0.60 2
rs1267634673
THRB
0.925 0.040 3 24127628 missense variant C/T snv 2
rs2048722
TPO
0.925 2 1492028 intron variant A/G snv 0.51 2
rs2280381 0.882 0.080 16 85985027 intron variant C/T snv 0.64 3
rs2276886
CXCL9
0.882 0.120 4 76007275 intron variant C/A;T snv 3
rs1061502
IRF7
0.882 0.160 11 614318 missense variant T/C snv 0.25 0.33 3
rs17593222
STAT3
0.925 0.120 17 42360972 intron variant C/G snv 6.1E-02 3
rs853326
TG
0.882 0.120 8 132897729 missense variant A/G snv 0.58 0.60 3
rs12492609
TMEM39A
0.882 0.040 3 119435715 intron variant C/T snv 0.14 3
rs7629750
TMEM39A
0.882 0.040 3 119455829 intron variant A/G snv 0.45 3
rs661561
TNFAIP3
0.882 0.200 6 137876194 intron variant A/C snv 0.62 0.50 3
rs2071400
TPO
0.882 0.120 2 1412867 intron variant C/T snv 0.11 3
rs4840568
BLK
0.882 0.160 8 11493510 intron variant G/A snv 0.32 4
rs1131665
IRF7
0.851 0.160 11 613208 missense variant T/C snv 0.25 0.33 4
rs17445836 0.851 0.320 16 85984057 intron variant G/A snv 0.15 5
rs6479778
ARID5B
0.827 0.200 10 61929318 intron variant T/C;G snv 5
rs2900180
C5-OT1
0.827 0.280 9 120944104 regulatory region variant T/A;C snv 5
rs745826707
RBM45
0.851 0.200 2 178112712 missense variant G/A;T snv 8.0E-06; 4.0E-06 5
rs2076740
TG
0.827 0.160 8 132971813 missense variant C/T snv 0.31 0.37 5
rs3788013
UBASH3A
0.851 0.240 21 42421219 intron variant C/A snv 0.44 5