Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs77375493
INSL6 ; JAK2
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs387907272
MYD88
0.572 0.520 3 38141150 stop lost T/C snv 5.2E-05 7.0E-06 73
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs3804100
TLR2
0.633 0.720 4 153704257 synonymous variant T/C snv 9.0E-02 6.7E-02 36
rs568408
IL12A ; IL12A-AS1
0.649 0.600 3 159995680 3 prime UTR variant G/A snv 0.16 29
rs9808753
IFNGR2
0.701 0.400 21 33415005 missense variant A/G snv 0.20 0.18 17
rs1494555
IL7R
0.790 0.120 5 35871088 missense variant G/A snv 0.64 0.72 8
rs497309
CYP21A2 ; C2
0.882 0.240 6 31924707 intron variant A/C;G snv 5
rs1250550
ZMIZ1
0.851 0.240 10 79300560 intron variant C/A snv 0.27 5
rs1439112
MGAT5
0.851 0.160 2 134305027 intron variant G/A snv 0.61 4
rs2425752
NCOA5
0.851 0.160 20 46073481 intron variant T/C snv 0.79 4
rs2777899
VMP1
0.851 0.160 17 59755030 intron variant T/A;G snv 4
rs1444766
KALRN
0.882 0.160 3 124206424 intron variant A/G;T snv 3
rs1323292
LOC105371664
0.882 0.160 1 192571891 intron variant G/A snv 0.86 3
rs928883
MIR155HG
0.882 0.160 21 25571713 intron variant A/G snv 0.83 3
rs1364229 0.925 0.200 16 62594871 upstream gene variant T/C snv 0.12 2
rs7382170 0.925 0.160 6 16970739 intergenic variant C/A snv 0.37 2
rs16947122
FBXW8
0.925 0.200 12 116928726 intron variant C/T snv 7.3E-02 2
rs2941509
IKZF3
0.925 0.160 17 39764941 3 prime UTR variant T/C snv 0.91 2
rs1107345
IL2RA
0.925 0.160 10 6045332 intron variant G/T snv 0.18 2
rs8021741
LOC107984652
0.925 0.160 14 75556057 intergenic variant T/G snv 0.30 2
rs6062314
ZBTB46
0.925 0.160 20 63778360 intron variant C/G;T snv 2
rs2922994 1.000 0.120 6 31368124 intron variant A/G snv 9.0E-02 1
rs9461741
BTNL2 ; TSBP1-AS1
1.000 0.120 6 32402810 intron variant G/C snv 3.8E-02 1
rs344550
C3
1.000 0.120 19 6682942 non coding transcript exon variant C/G snv 0.64 1