Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12931878
CLEC16A
1.000 0.120 16 10948337 intron variant A/G snv 0.14 1
rs12923849
CLEC16A
1.000 0.120 16 10968140 intron variant G/A snv 0.13 1
rs17229044
CLEC16A
1.000 0.120 16 10969079 intron variant C/T snv 0.16 2
rs13330041
CLEC16A
1.000 0.120 16 10994951 intron variant G/A snv 0.25 2
rs713041
GPX4
0.776 0.400 19 1106616 stop gained T/A;C snv 4.2E-06; 0.58 16
rs725613
CLEC16A
0.851 0.240 16 11075826 intron variant T/G snv 0.42 4
rs2041670
CLEC16A
0.851 0.280 16 11080795 intron variant G/A;C snv 4
rs7200786
CLEC16A
0.882 0.200 16 11083944 intron variant A/G snv 0.59 3
rs4849135
ACOXL
1.000 0.120 2 110857502 intron variant T/G snv 0.67 1
rs12708716
CLEC16A
0.807 0.320 16 11086016 intron variant A/G snv 0.37 7
rs886125 1.000 0.120 12 110927520 intergenic variant A/G snv 0.57 1
rs12924729
CLEC16A
0.882 0.200 16 11093926 intron variant G/A snv 0.34 3
rs12917716
CLEC16A
0.851 0.200 16 11095291 intron variant G/C snv 0.51 4
rs12599402
CLEC16A
0.925 0.160 16 11096031 intron variant T/C snv 0.51 2
rs12927355
CLEC16A
0.882 0.240 16 11100914 intron variant C/A;T snv 0.29 3
rs998592
CLEC16A
0.925 0.160 16 11105821 intron variant C/T snv 0.39 2
rs9933507
CLEC16A
1.000 0.120 16 11107571 intron variant T/C snv 0.46 1
rs1265564
CUX2
1.000 0.120 12 111270654 non coding transcript exon variant A/C snv 0.30 4
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs2903692
CLEC16A
0.807 0.360 16 11144926 intron variant G/A snv 0.33 6
rs17673553
CLEC16A
1.000 0.120 16 11148049 intron variant A/G snv 0.18 2
rs6498169
CLEC16A
0.807 0.280 16 11155472 non coding transcript exon variant G/A snv 0.66 6
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs2234702
HSPB2 ; CRYAB ; HSPB2-C11orf52
1.000 0.120 11 111912374 intron variant G/A;C snv 1
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 18