Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11865121
CLEC16A
1.000 0.080 16 11072831 intron variant C/A snv 0.40 1
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
rs12708716
CLEC16A
0.807 0.320 16 11086016 intron variant A/G snv 0.37 7
rs12927355
CLEC16A
0.882 0.240 16 11100914 intron variant C/A;T snv 0.29 3
rs6498160
CLEC16A
1.000 0.080 16 11105590 intron variant T/C snv 0.51 1
rs998592
CLEC16A
0.925 0.160 16 11105821 intron variant C/T snv 0.39 2
rs2080272
CLEC16A
1.000 0.080 16 11117696 intron variant A/C;G snv 1
rs7184083
CLEC16A ; LOC105371081
1.000 0.080 16 11134057 intron variant A/G snv 0.72 1
rs6498168
CLEC16A
1.000 0.080 16 11141273 intron variant T/G snv 0.71 1
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
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
rs17174870
MERTK
1.000 0.080 2 111907624 intron variant C/T snv 0.24 1
rs4780346 1.000 0.080 16 11194949 upstream gene variant G/A snv 0.19 1
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 18
rs4807569
SBNO2
0.925 0.120 19 1123379 intron variant A/C snv 0.25 2
rs11074956 0.925 0.160 16 11243864 downstream gene variant G/T snv 0.34 2
rs243324
RMI2 ; LOC105371082
1.000 0.080 16 11261113 intron variant A/G snv 0.51 1
rs17561
IL1A
0.672 0.560 2 112779646 missense variant C/A snv 0.27 0.26 23
rs1800587
IL1A
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs423674
RMI2 ; LOC105371082
0.925 0.120 16 11279548 intron variant G/T snv 0.18 3
rs1143634
IL1B
0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52