Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs352139
TLR9
0.732 0.320 3 52224356 intron variant T/C snv 0.51 0.54 18
rs763780
IL17F
0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs2397084
IL17F
0.716 0.480 6 52237046 missense variant T/C snv 6.7E-02 6.1E-02 14
rs1364989 0.925 0.160 4 54145602 intron variant T/C snv 0.73 2
rs2246614
CDHR5
0.882 0.160 11 619789 missense variant T/G snv 0.63 0.59 3
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs329498
PELI1
0.882 0.200 2 64100410 synonymous variant G/A;C;T snv 8.0E-06; 0.34 3
rs7692514 0.925 0.160 4 65276878 intergenic variant G/A;C snv 2
rs4984
LOC105374794 ; ADD2
0.925 0.160 2 70673271 synonymous variant G/A snv 0.12 0.15 3
rs117026326
LOC101926943 ; GTF2I
0.752 0.440 7 74711703 intron variant C/T snv 1.3E-02 10
rs8091180
NFATC1
1.000 0.160 18 79404243 intron variant G/A snv 0.46 3
rs3824662
GATA3
0.752 0.320 10 8062245 intron variant C/A;T snv 11
rs11981433
PON2
0.882 0.240 7 95425028 intron variant T/C;G snv 4
rs6056923
PAK5
1.000 0.160 20 9840271 intron variant T/C snv 0.10 1