Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs6570507
ADGRG6
0.827 0.240 6 142358435 intron variant G/A snv 0.47 13
rs864745
JAZF1
0.763 0.320 7 28140937 intron variant T/C snv 0.41 12
rs2247056
LOC112267902 ; HLA-B ; LINC02571
0.882 0.160 6 31297713 intron variant T/C snv 0.80 11
rs3791679
EFEMP1 ; LOC112268416
0.925 0.120 2 55869757 intron variant A/G snv 0.20 11
rs2516448 0.827 0.120 6 31422633 intron variant T/C;G snv 10
rs1182188
GNA12
0.827 0.120 7 2830351 intron variant T/C snv 0.26 8
rs6569648
L3MBTL3
1.000 0.080 6 130027974 intron variant C/T snv 0.84 7
rs7759938
LIN28B-AS1
0.925 0.120 6 104931079 intron variant C/T snv 0.62 7
rs11082304
CABLES1
18 23141009 intron variant G/C;T snv 6
rs1812175
HHIP-AS1 ; HHIP
4 144653692 intron variant A/G snv 0.79 6
rs2284746
MFAP2
1 16980180 intron variant C/A;G snv 6
rs314277
LIN28B
0.925 0.080 6 104959787 intron variant A/C;G;T snv 6
rs7741741
ADGRG6
0.925 0.040 6 142334664 intron variant T/A;G snv 6
rs849141
JAZF1
0.851 0.240 7 28145472 intron variant A/G snv 0.78 6
rs1635852
JAZF1
0.882 0.160 7 28149792 intron variant T/C snv 0.42 5
rs2282978
LOC112268009 ; CDK6
7 92635096 intron variant T/C snv 0.38 5
rs4896582
ADGRG6
6 142382740 intron variant G/A snv 0.50 5
rs10010325
TET2 ; TET2-AS1
1.000 0.040 4 105185196 intron variant C/A;G;T snv 4
rs10512248
PTCH1
0.925 0.120 9 95497421 intron variant T/A;G snv 4
rs11891311
UGT1A8 ; UGT1A3 ; UGT1A5 ; UGT1A9 ; UGT1A10 ; UGT1A4 ; UGT1A6 ; UGT1A7
2 233730664 intron variant G/A snv 0.42 4
rs12982744
DOT1L
0.925 0.040 19 2177194 intron variant C/A;G;T snv 4
rs1330
NUCB2
1.000 0.080 11 17294482 intron variant C/T snv 0.30 4
rs1344674
ZBTB38
3 141406344 intron variant A/G snv 0.55 4
rs1490384 6 126530014 intron variant C/G;T snv 4