Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4958881
TNIP1
0.827 0.280 5 151070675 intron variant T/C snv 0.21 7
rs2230911
LOC105370032 ; P2RX7
0.807 0.360 12 121177328 missense variant C/G snv 0.14 0.12 6
rs6590330 0.851 0.280 11 128441164 intergenic variant G/A;T snv 5
rs1556445736
COL4A5
0.925 0.200 X 108667167 synonymous variant A/G snv 5
rs10127939
FCGR3A
0.851 0.160 1 161548543 missense variant A/C;T snv 4.3E-02; 5.5E-02 5
rs3766379
CD244
0.851 0.320 1 160837925 intron variant T/C snv 0.57 4
rs104886308
COL4A5
0.851 0.160 X 108696350 missense variant G/A;C;T snv 2.2E-05 4
rs6682654
CD244
0.882 0.320 1 160839213 intron variant G/A snv 0.45 3
rs35366573
CD46
0.882 0.120 1 207785101 missense variant C/T snv 1.5E-02 1.5E-02 3
rs13385731
RASGRP3
0.882 0.200 2 33476823 intron variant T/C snv 6.3E-02 3
rs10847697
SLC15A4
0.882 0.200 12 128814840 synonymous variant G/A snv 0.13 9.1E-02 3
rs2326369
MAVS
0.925 0.160 20 3862337 synonymous variant C/T snv 9.2E-02 0.11 2
rs1800897
PAX2
0.925 0.240 10 100809115 synonymous variant C/T snv 7.4E-02 0.13 2
rs3124954
FCN2
1.000 0.080 9 134881650 intron variant C/T snv 0.32 1
rs17857295
MAVS
1.000 0.080 20 3857794 stop gained C/A;G;T snv 1.6E-05; 0.29; 4.0E-06 1