Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs184003
AGER
0.724 0.400 6 32182519 intron variant C/A snv 0.12 0.12 15
rs1861494
IFNG-AS1 ; IFNG
0.716 0.400 12 68157629 intron variant C/T snv 0.75 15
rs2670660
NLRP1
0.708 0.400 17 5615686 intron variant A/G snv 0.41 15
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 14
rs2069718
IFNG ; IFNG-AS1
0.742 0.320 12 68156382 intron variant A/G;T snv 0.50 14
rs4646536
CYP27B1
0.724 0.440 12 57764205 intron variant A/G snv 0.38 0.32 14
rs7216389
GSDMB
0.732 0.440 17 39913696 intron variant C/T snv 0.60 14
rs10774625
ATXN2
0.763 0.320 12 111472415 intron variant A/G snv 0.66 13
rs10865710
PPARG
0.763 0.360 3 12311699 intron variant C/G snv 0.25 13
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 13
rs2855812
MICB
0.790 0.360 6 31504943 intron variant G/T snv 0.23 13
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T snv 13
rs7044343
LOC107987046 ; IL33
0.752 0.520 9 6254208 intron variant C/T snv 0.51 13
rs17293632
SMAD3
0.763 0.240 15 67150258 intron variant C/T snv 0.17 12
rs2227284
IL4
0.732 0.480 5 132677033 intron variant T/C;G snv 12
rs324011
STAT6
0.742 0.360 12 57108399 intron variant C/T snv 0.32 12
rs10036748
TNIP1
0.752 0.360 5 151078585 intron variant C/A;T snv 11
rs2301436
FGFR1OP
0.752 0.320 6 167024500 intron variant C/T snv 0.42 11
rs2738783
RTEL1 ; RTEL1-TNFRSF6B
0.763 0.160 20 63677259 intron variant T/G snv 0.85 11
rs4969170
LOC101928674
0.752 0.440 17 78364457 intron variant A/C;G snv 0.54 11
rs6908425
CDKAL1
0.752 0.320 6 20728500 intron variant T/C snv 0.78 11
rs8076131
ORMDL3
0.790 0.200 17 39924659 intron variant G/A;C snv 11
rs10507391
ALOX5AP
0.776 0.320 13 30737959 intron variant A/T snv 0.52 10
rs10877012
CYP27B1 ; METTL1
0.763 0.280 12 57768302 intron variant G/C;T snv 10
rs11465804
IL23R
0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 10