Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs2292239
ERBB3
0.742 0.480 12 56088396 intron variant T/G snv 0.65 13
rs3825932
CTSH
0.827 0.360 15 78943104 intron variant T/C snv 0.50 6
rs2269067
C5
0.827 0.360 9 120974762 intron variant G/C snv 0.20 0.30 5
rs12267418
MALRD1
0.882 0.280 10 19425625 intron variant G/A snv 0.18 3
rs16999051
PCSK2
0.882 0.280 20 17380837 intron variant C/T snv 0.13 3
rs11014284
CACNB2
0.925 0.240 10 18451155 intron variant T/G snv 0.20 2
rs2236624
ADORA2A-AS1 ; SPECC1L-ADORA2A ; ADORA2A
0.925 0.200 22 24440056 intron variant T/C snv 0.80 2
rs3917779
SELP
0.925 0.280 1 169601610 intron variant G/A snv 0.22 2
rs4822489
SPECC1L-ADORA2A ; ADORA2A ; ADORA2A-AS1
0.925 0.200 22 24437792 intron variant T/G snv 0.48 2
rs869312979
POLA1
1.000 0.160 X 24726579 intron variant A/G snv 1
rs918519 1.000 0.160 5 159399349 intron variant A/G snv 0.78 1
rs6921438 0.776 0.360 6 43957870 intergenic variant G/A;C snv 10
rs10738760 0.807 0.320 9 2691186 regulatory region variant A/G snv 0.56 7
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1800470
TGFB1
0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs4994
ADRB3
0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs1800471
TGFB1
0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 48
rs1063856
VWF
0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 14
rs17611
C5
0.732 0.480 9 121006922 missense variant C/T snv 0.47 0.36 14
rs6133
SELP
0.851 0.280 1 169596108 missense variant C/A;G snv 0.12 4