Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1926447
CPB2 ; CPB2-AS1
0.807 0.440 13 46055809 missense variant A/G snv 0.74 0.77 11
rs2977324 8 75804502 intergenic variant T/G snv 0.77 1
rs1154988 3 136206349 upstream gene variant T/A snv 0.76 7
rs174877
TANGO2
22 20057896 intron variant T/A;C snv 0.75 1
rs2472610
NPC1
18 23558901 intron variant T/C snv 0.73 1
rs4746172
VCL
10 74096084 intron variant C/T snv 0.73 3
rs4865796
ARL15
1.000 0.080 5 53976834 intron variant G/A snv 0.72 3
rs3821843
CACNA1D
3 53523985 intron variant G/A snv 0.72 3
rs11605518 11 13248667 intergenic variant A/G snv 0.72 1
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs3937593
LOC105374843
2 85983150 intergenic variant C/T snv 0.71 1
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21
rs1801253
ADRB1
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 34
rs4580704
CLOCK
0.790 0.200 4 55460540 intron variant G/C snv 0.69 13
rs4387287
STN1
10 103918139 5 prime UTR variant A/C snv 0.69 4
rs2010963
VEGFA
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs4917
AHSG
0.790 0.160 3 186619924 missense variant T/C snv 0.68 0.68 9
rs7685862
ENPEP
4 110467945 intron variant C/A snv 0.68 1
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs762551
CYP1A2
0.701 0.400 15 74749576 intron variant C/A snv 0.67 23
rs151290
KCNQ1
1.000 0.080 11 2800385 intron variant A/C snv 0.67 2
rs4638289
SAA1
1.000 0.080 11 18264227 upstream gene variant A/T snv 0.67 2
rs2246490 14 103517957 downstream gene variant G/T snv 0.67 1
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62