Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs2670660
NLRP1
0.708 0.400 17 5615686 intron variant A/G snv 0.41 15
rs7708392
TNIP1
0.732 0.400 5 151077924 intron variant G/C snv 0.44 13
rs10036748
TNIP1
0.752 0.360 5 151078585 intron variant C/A;T snv 11
rs3819025
IL17A
0.752 0.480 6 52186476 intron variant G/A snv 0.13 8.5E-02 11
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
rs6677604
CFH
0.827 0.200 1 196717788 intron variant G/A snv 0.23 7
rs3766379
CD244
0.851 0.320 1 160837925 intron variant T/C snv 0.57 4
rs13385731
RASGRP3
0.882 0.200 2 33476823 intron variant T/C snv 6.3E-02 3
rs6682654
CD244
0.882 0.320 1 160839213 intron variant G/A snv 0.45 3
rs3124954
FCN2
1.000 0.080 9 134881650 intron variant C/T snv 0.32 1
rs6590330 0.851 0.280 11 128441164 intergenic variant G/A;T snv 5
rs5744168
TLR5
0.701 0.480 1 223111858 stop gained G/A snv 5.3E-02 4.4E-02 18
rs17857295
MAVS
1.000 0.080 20 3857794 stop gained C/A;G;T snv 1.6E-05; 0.29; 4.0E-06 1
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs763780
IL17F
0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs1222213359
VEGFA
0.574 0.720 6 43770966 missense variant G/A snv 62
rs3743930
MEFV
0.611 0.720 16 3254626 missense variant C/G;T snv 7.1E-02 43
rs800292
CFH
0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 33
rs1718119
LOC105370032 ; P2RX7
0.689 0.520 12 121177300 missense variant G/A;T snv 0.35; 4.0E-06 21
rs1065489
CFH
0.695 0.440 1 196740644 missense variant G/T snv 0.20 0.15 19
rs1143679
ITGAM
0.732 0.520 16 31265490 missense variant G/A snv 9.7E-02 0.11 14
rs12150220
NLRP1
0.724 0.360 17 5582047 missense variant A/T snv 0.37 0.33 14