Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17246129 2 226395248 intergenic variant G/A;T snv 1
rs2005172
GH1
17 63918895 intron variant A/C;T snv 1
rs2163832
SLC44A2
19 10635088 intron variant T/A;C;G snv 0.73; 4.0E-06 1
rs2408508 12 46336817 intergenic variant T/A;C snv 1
rs2474944 1 118342903 intergenic variant T/A;C;G snv 1
rs2507838
GLYAT
11 58705326 intron variant C/A;G snv 1
rs2618152
DIRC3
2 217447875 intron variant G/A;C snv 1
rs2643672
LOC105369944
12 102648521 intergenic variant G/A;C snv 1
rs2923097
CAND1.11 ; AMPD3
11 10343497 intron variant A/G;T snv 1
rs34287
PIK3R1
5 68289315 intron variant G/A;C snv 1
rs35957220
GNA12 ; AMZ1
7 2772998 intron variant C/A;G snv 1
rs3822742
CXXC5
5 139679432 intron variant C/A;T snv 1
rs397858888 18 60165624 downstream gene variant C/-;CC;CCC delins 1
rs4269347
LYRM2 ; ANKRD6
6 89587169 intron variant C/G;T snv 1
rs56074300 15 38221661 intron variant C/A;G snv 1
rs5752989
MTMR3
22 29969791 intron variant G/A;T snv 1
rs58066158
LOC105374493
4 12899739 intergenic variant G/A;T snv 1
rs60401266
LNCTAM34A ; MIR34AHG
1 9192362 intron variant G/A;T snv 1
rs62058277
LINC01572
16 72248051 intron variant T/C;G snv 1
rs62165906
VAMP8
2 85573985 intron variant C/A;G;T snv 1
rs6946091 7 150987258 upstream gene variant A/C;G snv 1
rs73619441
DIDO1
20 62933549 intron variant T/C;G snv 1
rs76798800
DCST2
1 155022502 intron variant G/A;T snv 1
rs8047465 16 86383718 regulatory region variant T/A;C;G snv 1
rs933807
VPS13C
15 61982741 intron variant G/A;C snv 1