Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11066001
BRAP
0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 15
rs2238151
ALDH2
1.000 0.040 12 111774029 intron variant T/C snv 0.52 3
rs2339840
ALDH2
1.000 0.040 12 111817137 3 prime UTR variant C/T snv 3.4E-02 2
rs9604365 13 111922883 intergenic variant G/A snv 0.82 1
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 18
rs12037987
WNT2B
1 112500200 intron variant T/C snv 8.6E-02 2
rs34311906
ANK2
1.000 0.080 4 112810934 intergenic variant T/C snv 0.43 2
rs549858786
IL1B
0.790 0.320 2 112836807 5 prime UTR variant T/A snv 10
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 22
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs11681884 2 113090051 downstream gene variant C/T snv 0.21 1
rs367732974
F7
0.790 0.360 13 113105788 5 prime UTR variant G/A snv 8.9E-05 2.8E-05 9
rs549591993
F7
0.776 0.400 13 113105794 5 prime UTR variant C/A snv 4.0E-04 2.8E-05 12
rs201058276
F7
0.776 0.240 13 113118731 missense variant G/A;C snv 4.8E-05; 4.0E-06 11
rs380092
IL1RN
2 113131323 intron variant T/A snv 0.57 1
rs1290267513
TCF7L2
10 113146078 missense variant G/A snv 4.0E-06 7.1E-06 1
rs3024718
PROZ
13 113159539 intron variant A/G snv 0.17 1
rs3024778
PROZ
13 113160151 stop gained G/A;C;T snv 4.0E-06; 2.0E-05 1
rs3024731
PROZ
0.925 0.080 13 113164394 intron variant A/C;T snv 3
rs3024772
PCID2 ; PROZ
13 113171786 missense variant G/A;C snv 2.4E-02; 4.0E-06 1
rs11196288 1.000 0.080 10 113297684 regulatory region variant A/G snv 5.5E-02 2
rs12122341 1.000 0.080 1 115113069 regulatory region variant C/G snv 0.19 2
rs35436 1.000 0.080 12 115116718 intergenic variant C/T snv 0.40 5
rs6330
NGF ; NGF-AS1
0.763 0.240 1 115286692 missense variant G/A snv 0.37 0.36 12
rs113092656 0.882 0.120 6 11615072 intergenic variant G/A snv 2.6E-02 5