Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10206753
IL18R1 ; IL1RL1
1.000 0.080 2 102351902 missense variant T/C;G snv 0.34; 4.0E-06 2
rs10208293
IL1RL1 ; IL18R1
0.882 0.160 2 102349850 intron variant G/A snv 0.33 4
rs10211025 1.000 0.080 2 41801493 intergenic variant A/G snv 0.12 1
rs1022113606
SOD3
0.732 0.280 4 24800161 missense variant G/C snv 1.6E-04 2.1E-05 17
rs1023518
IRF1-AS1
1.000 0.080 5 132458080 intron variant G/T snv 0.26 1
rs10237103
GNAI1
1.000 0.080 7 80032911 intron variant C/T snv 0.11 1
rs10268774 1.000 0.080 7 82453122 intergenic variant T/C snv 3.2E-02 1
rs1031509
STAT4
1.000 0.080 2 191145463 intron variant T/G snv 0.64 1
rs1034395178
LZTR1
0.716 0.480 22 20996071 stop gained C/A;T snv 4.0E-06; 8.0E-06 33
rs1038770
SYNPO2
1.000 0.080 4 118953332 intron variant G/A snv 9.5E-02 1
rs1039559
TLR6 ; TLR1
1.000 0.080 4 38829975 intron variant G/A snv 0.62 2
rs10399805
CHI3L1
0.851 0.240 1 203186870 upstream gene variant G/A;T snv 7
rs10399931
CHI3L1
0.807 0.320 1 203186952 upstream gene variant T/A;C snv 6
rs10404342
ZNF71-SMIM17 ; ZNF71
1.000 0.080 19 56620870 intron variant C/A snv 0.17 1
rs10409962
SIGLEC8
1.000 0.080 19 51457686 missense variant A/G snv 0.12 0.21 1
rs10411428 1.000 0.080 19 52104512 intergenic variant C/T snv 0.18 1
rs10413947 1.000 0.080 19 9017666 upstream gene variant G/A;T snv 1
rs10414065 0.882 0.080 19 33230549 upstream gene variant C/T snv 5.5E-02 4
rs1041973
IL18R1 ; IL1RL1
1.000 0.080 2 102339008 missense variant C/A snv 0.23 0.30 1
rs1042658
CSF3
1.000 0.080 17 40017649 3 prime UTR variant C/G;T snv 1
rs1042711
ADRB2
0.827 0.120 5 148826785 5 prime UTR variant C/A;G;T snv 4.2E-06; 0.68 5
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
rs1042718
ADRB2
0.925 0.080 5 148827354 missense variant C/A;T snv 0.23; 4.0E-06 3
rs1043828
WDR36
1.000 0.080 5 111128310 3 prime UTR variant T/C;G snv 2