Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6056923
PAK5
1.000 0.160 20 9840271 intron variant T/C snv 0.10 1
rs6677604
CFH
0.827 0.200 1 196717788 intron variant G/A snv 0.23 7
rs1456896 0.882 0.200 7 50264865 upstream gene variant C/T snv 0.67 5
rs11203368
PADI4
0.925 0.200 1 17340013 intron variant C/T snv 0.57 3
rs329498
PELI1
0.882 0.200 2 64100410 synonymous variant G/A;C;T snv 8.0E-06; 0.34 3
rs1391441
TET2-AS1 ; TET2
0.763 0.240 4 105207603 intron variant G/A snv 0.70 11
rs172378
C1QA
0.790 0.240 1 22638945 synonymous variant A/G snv 0.49 0.51 11
rs11981433
PON2
0.882 0.240 7 95425028 intron variant T/C;G snv 4
rs2298804
FCER1A
0.851 0.240 1 159304102 missense variant A/G;T snv 6.6E-03 4
rs4958881
TNIP1
0.827 0.280 5 151070675 intron variant T/C snv 0.21 7
rs352139
TLR9
0.732 0.320 3 52224356 intron variant T/C snv 0.51 0.54 18
rs7848647
TNFSF15
0.732 0.320 9 114806766 upstream gene variant T/C snv 0.74 13
rs6478109
TNFSF15
0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 12
rs8193037
IL17A
0.752 0.320 6 52186311 upstream gene variant G/A;T snv 12
rs3824662
GATA3
0.752 0.320 10 8062245 intron variant C/A;T snv 11
rs2647012 0.790 0.320 6 32696681 intergenic variant T/C snv 0.64 7
rs292001
C1QA
0.807 0.320 1 22638465 intron variant G/A snv 0.54 6
rs7708392
TNIP1
0.732 0.400 5 151077924 intron variant G/C snv 0.44 13
rs28940579
MEFV
0.732 0.440 16 3243310 missense variant A/G;T snv 2.2E-03; 4.0E-06 13
rs117026326
LOC101926943 ; GTF2I
0.752 0.440 7 74711703 intron variant C/T snv 1.3E-02 10
rs5744168
TLR5
0.701 0.480 1 223111858 stop gained G/A snv 5.3E-02 4.4E-02 18
rs2397084
IL17F
0.716 0.480 6 52237046 missense variant T/C snv 6.7E-02 6.1E-02 14
rs396991
FCGR3A
0.742 0.480 1 161544752 missense variant A/C;G;T snv 0.33; 4.1E-06 14
rs11889341
STAT4
0.732 0.480 2 191079016 intron variant C/T snv 0.21 12
rs2004640
IRF5
0.662 0.520 7 128938247 splice donor variant T/G snv 0.52 26