Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
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
rs1263178238
VSIG10L
0.925 0.080 19 51338047 missense variant T/C snv 2.6E-05 4.9E-05 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
rs491603
AGO3
1.000 0.080 1 36066715 3 prime UTR variant T/A;C snv 2
rs62423175 0.925 0.080 6 61485463 intergenic variant G/A snv 2
rs7852462
TMOD1
0.925 0.080 9 97548219 intron variant C/A;T snv 2
rs9823696 0.925 0.080 3 184065565 downstream gene variant A/G;T snv 2
rs9918259
CEP72 ; TPPP
0.925 0.080 5 662977 3 prime UTR variant C/T snv 2.1E-03 2
rs11631094
SLC12A6
1.000 0.080 15 34332237 intron variant G/C;T snv 1