Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1015438
SALL1
16 51143606 intron variant G/A snv 0.19 1
rs1016162 3 102299 regulatory region variant C/T snv 0.36 1
rs10161821
LINC00375 ; LOC105370291
13 85129514 intergenic variant G/A;C;T snv 1
rs10164820 2 100433891 intergenic variant G/C snv 0.20 1
rs1016678 17 37514090 downstream gene variant A/G snv 0.72 1
rs10171320
LOC101928273
2 137928042 intergenic variant A/C snv 0.62 1
rs10177638 2 62659875 intron variant C/T snv 0.69 1
rs10183150
LONRF2
2 100322655 upstream gene variant A/G;T snv 1
rs10189857
BCL11A
1.000 0.080 2 60486100 intron variant A/G snv 0.42 6
rs10192369 2 160524377 intergenic variant G/A snv 0.45 2
rs10193498
MAP3K20-AS1 ; MAP3K20
2 173229617 intron variant A/C;T snv 0.32 1
rs10196515 2 153383795 intergenic variant C/A snv 0.82 1
rs10197780 2 62646060 intron variant T/C snv 0.78 1
rs1019914
SDK1
7 3672560 intron variant G/A;C snv 1
rs10202535
TMEM182
2 102957679 intron variant T/C snv 0.61 1
rs10205421
VRK2
2 58070529 intron variant G/A;C snv 1
rs10206657
LOC105373929
2 232597385 intron variant G/A snv 0.19 1
rs10208720
PKP4
2 158609502 intron variant T/G snv 0.83 1
rs10211312
LOC105374764 ; TMEM17
2 62466982 downstream gene variant A/C;T snv 1
rs1021469
AVIL
12 57814381 intron variant G/A snv 0.28 1
rs10215015
DGKB
7 14785984 intron variant A/G snv 0.26 1
rs10218999
LOC105376481
10 31076645 intron variant G/A snv 0.16 1
rs10223255 5 92705821 intergenic variant A/C;G snv 1
rs10232276
GRM8
7 126943467 intron variant T/C snv 0.23 1
rs10233848
LOC101927870 ; RELN
7 103482198 non coding transcript exon variant A/G snv 0.42 1