Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4683336
KRBOX1 ; ACKR2
3 42818461 intron variant C/T snv 0.61 1
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs17879702
HLA-DRB1
1.000 0.080 6 32584346 missense variant G/A snv 3.2E-02 5.7E-02 2
rs11025185
NAV2
11 19572259 intron variant G/A snv 2.4E-03 1
rs9522267 13 111544020 intergenic variant G/A snv 0.32 1
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1879026
TLR3
1.000 0.080 4 186079167 intron variant G/C;T snv 3
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs4696480
TLR2
0.716 0.400 4 153685974 intron variant T/A snv 0.45 19
rs12583006
TNFSF13B
0.807 0.320 13 108285104 intron variant T/A snv 0.21 8
rs641738
LOC112268246 ; TMC4 ; MBOAT7
0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
rs3804099
TLR2
0.627 0.680 4 153703504 synonymous variant T/C snv 0.40 0.48 40
rs3804100
TLR2
0.633 0.720 4 153704257 synonymous variant T/C snv 9.0E-02 6.7E-02 36
rs352139
TLR9
0.732 0.320 3 52224356 intron variant T/C snv 0.51 0.54 18
rs1047782
TDP2
6 24650503 3 prime UTR variant T/C;G snv 1
rs2149356
TLR4
0.742 0.360 9 117711921 intron variant T/G snv 0.54 14
rs368234815
IFNL4
0.742 0.280 19 39248514 frameshift variant TT/G;T delins 15