Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1046089
PRRC2A
0.882 0.200 6 31635190 missense variant G/A snv 0.36 0.40 4
rs76723693
G6PD
0.882 0.160 X 154533025 missense variant A/G snv 5.3E-04 1.5E-03 3
rs1463502008
PRH1-PRR4 ; PRH1 ; PRH2 ; PRR4
0.925 0.040 12 10930275 missense variant G/C snv 4.0E-06 2
rs993269089
ACOT7
1.000 0.040 1 6385564 missense variant A/C;T snv 4.0E-06 1
rs1800925
IL13 ; TH2LCRR
0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs34383331
MIF-AS1
0.882 0.040 22 23895892 non coding transcript exon variant T/A snv 0.19 0.18 3
rs1128503
ABCB1
0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs2070874
IL4
0.672 0.560 5 132674018 5 prime UTR variant C/T snv 0.28 0.28 27
rs9624472
ADORA2A ; ADORA2A-AS1 ; SPECC1L-ADORA2A
0.925 0.040 22 24438763 splice region variant A/G snv 0.10 2
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 47
rs1799964
LTA ; LOC100287329 ; TNF
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47
rs1800630
TNF ; LOC100287329 ; LTA
0.701 0.480 6 31574699 upstream gene variant C/A snv 0.14 17
rs5744454
TMCO6 ; CD14
1.000 0.040 5 140633982 upstream gene variant T/C;G snv 1