Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1003706636
NLRP3
1.000 0.120 1 247424639 missense variant T/C snv 1
rs1004819
C1orf141 ; IL23R
0.776 0.360 1 67204530 intron variant G/A snv 0.30 9
rs10128264
ZMIZ1
1.000 0.120 10 79200216 intron variant T/C snv 0.64 1
rs1018981
LOC105375246
1.000 0.120 7 41335525 intergenic variant C/A snv 3.2E-02 1
rs1042713
ADRB2
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs10431961
MMP25
1.000 0.120 16 3050094 synonymous variant C/G;T snv 4.0E-06; 0.32 1
rs10499194 0.752 0.400 6 137681500 intron variant C/T snv 0.24 10
rs1051266
SLC19A1
0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 41
rs10761744
JMJD1C
1.000 0.120 10 63341266 intron variant C/G;T snv 0.87 1
rs10761745
JMJD1C
0.882 0.240 10 63341311 intron variant G/C snv 0.87 3
rs10822050 0.724 0.240 10 62679011 downstream gene variant T/C snv 0.33 14
rs10919563
PTPRC
0.925 0.120 1 198731313 intron variant G/A snv 0.21 3
rs10931481
STAT4
0.827 0.240 2 191090126 intron variant G/A snv 0.66 5
rs10954213
IRF5
0.752 0.200 7 128949373 3 prime UTR variant G/A snv 0.58 11
rs10956445
CCDC26
1.000 0.120 8 128775730 intron variant T/C snv 0.20 1
rs10988542
FNBP1
0.724 0.240 9 129894985 intron variant G/A;C snv 14
rs11145763
CARD9
0.724 0.240 9 136369144 intron variant A/C;G;T snv 14
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs11225055
ANGPTL5
1.000 0.120 11 101900702 intron variant T/A;C snv 1
rs1127354
ITPA
0.667 0.400 20 3213196 missense variant C/A;G snv 7.5E-02 26
rs11466018
MEFV
0.827 0.200 16 3254739 missense variant A/G snv 6.6E-03 2.2E-03 7
rs114846446
LINC01250
0.724 0.240 2 2944140 intron variant G/A snv 9.5E-03 14
rs11580078
C1orf141 ; IL23R
0.724 0.240 1 67203951 intron variant C/A;G snv 14
rs117372389
NKD1
0.724 0.240 16 50634166 3 prime UTR variant G/T snv 1.1E-02 14