Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1485766
VEGFC ; LOC105377555
0.882 0.120 4 176689730 intron variant T/A;G snv 3
rs3844942 0.882 0.120 4 189571800 intergenic variant T/C snv 3
rs767864210
PDLIM5
0.882 0.120 4 94657500 missense variant G/A;T snv 8.0E-05 2.1E-05 3
rs10020432
AFP
0.925 0.080 4 73455883 3 prime UTR variant A/G snv 0.54 2
rs2298839
AFP
0.925 0.080 4 73445127 splice region variant A/G;T snv 0.54 2
rs6834059
AFP
0.925 0.080 4 73435958 intron variant C/G snv 0.23 2
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs2736098
TERT
0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs6897932
IL7R
0.683 0.560 5 35874473 missense variant C/T snv 0.23 0.21 25
rs10053538
HAVCR2
0.807 0.160 5 157110499 intron variant C/A;T snv 7
rs121918664
TERT
0.851 0.120 5 1254395 missense variant C/T snv 5.2E-05 9.1E-05 4
rs1346044973
TERT
0.851 0.160 5 1294158 missense variant G/A snv 1.1E-05 4
rs26907
RASGRF2
0.882 0.240 5 81069496 intron variant G/A;T snv 3
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1800730
HFE ; LOC108783645
0.649 0.480 6 26090957 missense variant A/T snv 1.0E-02 1.0E-02 32
rs1275561861
HLA-A
0.672 0.360 6 29944350 missense variant G/A snv 23
rs2596542
MICA-AS1 ; MICA
0.724 0.200 6 31398818 upstream gene variant C/T snv 0.41 18
rs3077
HLA-DPA1
0.701 0.440 6 33065245 3 prime UTR variant A/G snv 0.29 16
rs510432
ATG5
0.752 0.280 6 106326155 upstream gene variant T/C snv 0.57 11
rs548234
ATG5
0.763 0.360 6 106120159 intron variant C/T snv 0.76 11
rs143175221
LOC108783645 ; HFE
0.827 0.200 6 26092952 missense variant T/C snv 8.4E-04 5.6E-04 5
rs10945859
PRKN
0.882 0.120 6 162721570 intron variant T/C snv 0.17 3