Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12972991 1.000 0.080 19 39241107 upstream gene variant A/C snv 0.19 1
rs12980602 1.000 0.080 19 39262180 upstream gene variant T/C snv 0.25 1
rs2779180
PLIN3
1.000 0.080 19 4841139 intron variant A/G snv 0.37 1
rs4803223 1.000 0.080 19 39255579 upstream gene variant A/G snv 0.13 1
rs6139030
ITPA
1.000 0.080 20 3207087 upstream gene variant T/C snv 8.6E-02 1
rs8109886 1.000 0.080 19 39252122 upstream gene variant C/A snv 0.53 1
rs965469
C20orf194
1.000 0.080 20 3400902 intron variant T/C snv 0.20 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs758564400
REN
0.925 0.120 1 204156683 missense variant A/G snv 4.0E-06 5
rs3775291
TLR3
0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28 51
rs5743708
TLR2
0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs5743704
TLR2
0.763 0.240 4 153704799 missense variant C/A snv 2.8E-02 2.8E-02 9
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs58542926
TM6SF2
0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs1127354
ITPA
0.667 0.400 20 3213196 missense variant C/A;G snv 7.5E-02 26
rs7270101
ITPA
0.776 0.200 20 3213247 intron variant A/C snv 8.7E-02 9.7E-02 10
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs2230201
C3
0.882 0.200 19 6713280 synonymous variant C/G;T snv 0.19 3
rs6897932
IL7R
0.683 0.560 5 35874473 missense variant C/T snv 0.23 0.21 25
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs8103142
IFNL3
0.882 0.120 19 39244466 missense variant T/C snv 0.29 0.40 4
rs28416813
IFNL3
1.000 0.080 19 39245004 5 prime UTR variant C/G snv 0.31 0.39 1
rs11854484
SLC28A2 ; LOC101928414
0.925 0.120 15 45253280 missense variant C/T snv 0.47 0.45 2
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214