Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs397507545
PTPN11
0.708 0.560 12 112489083 missense variant G/A;C snv 4.0E-06 20
rs324011
STAT6
0.742 0.360 12 57108399 intron variant C/T snv 0.32 12
rs181181503
LOC100507377
0.851 0.160 12 74276187 intron variant T/C snv 1.5E-03 4
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs3135932
IL10RA
0.677 0.480 11 117993348 missense variant A/G snv 0.13 0.11 23
rs7120118
NR1H3
0.716 0.360 11 47264739 intron variant T/C snv 0.38 18
rs360719
IL18 ; LOC107987164 ; TEX12
0.790 0.480 11 112165426 non coding transcript exon variant A/G snv 0.25 7
rs11039155
NR1H3
0.827 0.400 11 47259211 5 prime UTR variant G/A snv 0.14 0.12 6
rs4525246
GRAMD1B
0.851 0.160 11 123524538 intron variant G/A;C snv 4
rs7111520
POU2AF1
1.000 0.120 11 111378886 intron variant G/A snv 0.58 1
rs1801157
CXCL12
0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16 46
rs12917
MGMT ; LOC105378560
0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 45
rs2308321
MGMT
0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02 29
rs7895833 0.742 0.440 10 67863299 upstream gene variant G/A;C snv 12
rs2308327
MGMT
0.790 0.280 10 129766906 missense variant A/G snv 9.4E-02 8.7E-02 10
rs7069102
SIRT1
0.790 0.440 10 67903362 intron variant C/G snv 0.64 10
rs2273773
SIRT1
0.790 0.360 10 67906841 synonymous variant T/C snv 0.11 7.1E-02 9
rs3781093
GATA3
0.882 0.120 10 8059964 intron variant T/C snv 0.19 3
rs1244186
GATA3-AS1 ; GATA3
1.000 0.120 10 8050720 non coding transcript exon variant T/A;C snv 1
rs485411
GATA3-AS1 ; GATA3
1.000 0.120 10 8051222 non coding transcript exon variant T/A;C;G snv 0.81 1
rs501764
GATA3-AS1 ; GATA3
1.000 0.120 10 8051071 non coding transcript exon variant G/T snv 0.87 0.86 1
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs77375493
INSL6 ; JAK2
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs182123615
JAK2 ; INSL6
0.807 0.200 9 5070058 splice region variant T/C snv 3.6E-04 1.1E-03 7