Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3758391
SIRT1
0.742 0.480 10 67883584 upstream gene variant T/C snv 0.64 11
rs3766379
CD244
0.851 0.320 1 160837925 intron variant T/C snv 0.57 4
rs2004640
IRF5
0.662 0.520 7 128938247 splice donor variant T/G snv 0.52 26
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs6682654
CD244
0.882 0.320 1 160839213 intron variant G/A snv 0.45 3
rs7708392
TNIP1
0.732 0.400 5 151077924 intron variant G/C snv 0.44 13
rs2670660
NLRP1
0.708 0.400 17 5615686 intron variant A/G snv 0.41 15
rs800292
CFH
0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 33
rs12150220
NLRP1
0.724 0.360 17 5582047 missense variant A/T snv 0.37 0.33 14
rs3124954
FCN2
1.000 0.080 9 134881650 intron variant C/T snv 0.32 1
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs4917014 0.807 0.360 7 50266267 upstream gene variant T/G snv 0.26 8
rs6677604
CFH
0.827 0.200 1 196717788 intron variant G/A snv 0.23 7
rs11864909
PDILT
0.851 0.160 16 20389517 intron variant C/T snv 0.23 7
rs4958881
TNIP1
0.827 0.280 5 151070675 intron variant T/C snv 0.21 7
rs1065489
CFH
0.695 0.440 1 196740644 missense variant G/T snv 0.20 0.15 19
rs1800897
PAX2
0.925 0.240 10 100809115 synonymous variant C/T snv 7.4E-02 0.13 2
rs2230911
LOC105370032 ; P2RX7
0.807 0.360 12 121177328 missense variant C/G snv 0.14 0.12 6
rs1143679
ITGAM
0.732 0.520 16 31265490 missense variant G/A snv 9.7E-02 0.11 14
rs2326369
MAVS
0.925 0.160 20 3862337 synonymous variant C/T snv 9.2E-02 0.11 2
rs10847697
SLC15A4
0.882 0.200 12 128814840 synonymous variant G/A snv 0.13 9.1E-02 3
rs3819025
IL17A
0.752 0.480 6 52186476 intron variant G/A snv 0.13 8.5E-02 11
rs763780
IL17F
0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs13385731
RASGRP3
0.882 0.200 2 33476823 intron variant T/C snv 6.3E-02 3
rs2397084
IL17F
0.716 0.480 6 52237046 missense variant T/C snv 6.7E-02 6.1E-02 14