Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6214
LINC02456 ; HELLPAR ; IGF1
0.672 0.400 12 102399791 3 prime UTR variant C/T snv 0.45 26
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 20
rs3088440
CDKN2A ; CDKN2A-DT
0.776 0.240 9 21968160 3 prime UTR variant G/A snv 0.13 12
rs9257809
OR12D3 ; OR5V1
0.790 0.320 6 29388554 intron variant A/G snv 5.8E-02 10
rs2178146 0.827 0.080 16 86430089 downstream gene variant T/C snv 0.31 8
rs11789015
BARX1
0.882 0.080 9 93953746 intron variant A/C;G snv 6
rs2687201 0.925 0.080 3 70879779 intergenic variant A/C;G snv 6
rs3784262
ALDH1A2
0.882 0.160 15 57960908 intron variant T/A;C snv 6
rs9936833 0.882 0.160 16 86369512 intergenic variant C/T snv 0.64 6
rs10419226
CRTC1
0.925 0.080 19 18692362 intron variant T/G snv 0.67 5
rs4800353 0.925 0.080 18 22074176 intergenic variant A/G snv 0.30 5
rs7632500
LOC107986152
0.925 0.080 3 168007561 downstream gene variant A/G snv 0.17 5
rs11901649
APOB
0.882 0.080 2 21027351 intron variant G/A;C;T snv 3
rs4676893 0.882 0.080 3 70868488 intergenic variant A/T snv 0.61 3
rs7255
GDF7
0.925 0.080 2 20679060 3 prime UTR variant T/A;C snv 3
rs10108511
LINC00208
0.925 0.080 8 11578007 non coding transcript exon variant T/A;C snv 2
rs1247942 0.925 0.080 12 114235918 downstream gene variant G/A;C snv 2
rs17451754
CFTR
0.925 0.080 7 117616658 intron variant G/A snv 0.10 2
rs17749155
MSRA
0.925 0.080 8 10210563 intron variant G/A snv 0.16 2
rs1979654 0.925 0.080 16 86363229 TF binding site variant G/C snv 0.55 2
rs199620551
CRTC1
0.925 0.080 19 18693485 intron variant G/- del 9.2E-02 2
rs2464469
LOC283665 ; ALDH1A2
0.925 0.080 15 58069827 intron variant G/A snv 0.65 2
rs2518720
CDKN2A
0.925 0.080 9 21978980 intron variant C/T snv 0.43 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