Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 20
rs2178146 0.827 0.080 16 86430089 downstream gene variant T/C snv 0.31 8
rs2687201 0.925 0.080 3 70879779 intergenic variant A/C;G snv 6
rs9936833 0.882 0.160 16 86369512 intergenic variant C/T snv 0.64 6
rs4800353 0.925 0.080 18 22074176 intergenic variant A/G snv 0.30 5
rs4676893 0.882 0.080 3 70868488 intergenic variant A/T snv 0.61 3
rs1247942 0.925 0.080 12 114235918 downstream gene variant G/A;C snv 2
rs1979654 0.925 0.080 16 86363229 TF binding site variant G/C snv 0.55 2
rs2687202 0.925 0.080 3 70880832 regulatory region variant T/C snv 0.64 2
rs2701108 0.925 0.160 12 114236456 downstream gene variant T/C snv 0.35 2
rs62423175 0.925 0.080 6 61485463 intergenic variant G/A snv 2
rs9823696 0.925 0.080 3 184065565 downstream gene variant A/G;T snv 2
rs2671828 1.000 0.080 17 35404745 upstream gene variant T/C snv 0.55 1
rs3776082 1.000 0.080 5 150164482 upstream gene variant G/A;C snv 1
rs4769585 1.000 0.080 13 27976441 downstream gene variant C/T snv 0.39 1
rs6449586 1.000 0.080 5 51339044 intergenic variant C/T snv 0.64 1
rs491603
AGO3
1.000 0.080 1 36066715 3 prime UTR variant T/A;C snv 2
rs3784262
ALDH1A2
0.882 0.160 15 57960908 intron variant T/A;C snv 6
rs66725070
ALDH1A2
1.000 0.080 15 57975219 intron variant ACAT/- delins 0.35 1
rs11901649
APOB
0.882 0.080 2 21027351 intron variant G/A;C;T snv 3
rs11789015
BARX1
0.882 0.080 9 93953746 intron variant A/C;G snv 6
rs2518720
CDKN2A
0.925 0.080 9 21978980 intron variant C/T snv 0.43 2
rs3088440
CDKN2A ; CDKN2A-DT
0.776 0.240 9 21968160 3 prime UTR variant G/A snv 0.13 12
rs717746
CDX1
1.000 0.080 5 150176995 intron variant T/A;C;G snv 1
rs3812863
CDX2
1.000 0.080 13 27971131 upstream gene variant G/A snv 0.48 1