Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs1800796
IL6-AS1 ; STEAP1B ; IL6
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs8193036
IL17A
0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 21
rs7096206
MBL2
0.708 0.480 10 52771925 upstream gene variant G/A;C;T snv 17
rs2606345
CYP1A1
0.732 0.360 15 74724835 intron variant C/A snv 0.46 16
rs61330082
NAMPT
0.732 0.320 7 106286419 upstream gene variant G/A snv 0.22 13
rs4957796
FER
0.851 0.120 5 109066439 intron variant T/C snv 0.16 5
rs7744
MYD88
0.827 0.160 3 38142530 3 prime UTR variant A/G snv 0.13 5
rs3774934
NFKB1
0.851 0.080 4 102506319 intron variant A/C;G;T snv 4
rs11137480
S1PR3 ; C9orf47
0.882 0.120 9 88989662 upstream gene variant G/C snv 0.37 3
rs1320896171
PAFAH1B1
0.882 0.120 17 2680294 missense variant C/T snv 7.0E-06 3
rs7022797
C9orf47 ; S1PR3
0.882 0.120 9 88989548 upstream gene variant T/G snv 0.38 3
rs1042689672
SFTPA2
0.925 0.080 10 79557504 missense variant A/G snv 7.0E-06 2
rs7692976
EGF
1.000 0.040 4 109990411 intron variant A/G;T snv 2
rs10905928
CELF2
1.000 0.040 10 11300924 intron variant C/A snv 0.21 1
rs1190286
POPDC3 ; BVES-AS1
1.000 0.040 6 105163071 intron variant C/T snv 0.66 1
rs13402990
C2orf42 ; TIA1
1.000 0.040 2 70231632 intron variant A/T snv 9.7E-03 1
rs2298991
EGF
1.000 0.040 4 109970856 intron variant T/A;G snv 1
rs2515475
ANGPT2 ; MCPH1
1.000 0.040 8 6530918 intron variant C/T snv 0.19 1
rs2592178
C2orf42 ; TIA1
1.000 0.040 2 70245350 intron variant G/A snv 0.27 1
rs3814634
CELF2 ; CELF2-AS2
1.000 0.040 10 11099442 splice region variant G/T snv 0.37 1
rs516651
EGLN1
1.000 0.040 1 231406910 intron variant C/T snv 0.15 1
rs6533485
EGF
1.000 0.040 4 110006407 intron variant G/C snv 0.61 1
rs672961
LRRC7
1.000 0.040 1 70101505 intron variant C/G snv 0.99 1
rs7068124
CELF2
1.000 0.040 10 11023453 intron variant T/C;G snv 1