Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9999820
NPY2R
0.925 0.080 4 155197173 intron variant A/G snv 0.66 1
rs9999653
NMU
1.000 0.080 4 55632082 intron variant C/T snv 0.51 1
rs999947969
CD36
0.827 0.080 7 80671145 synonymous variant C/T snv 7
rs999905
NTRK3
1.000 0.040 15 88020640 intron variant G/A;C snv 1
rs999885
AP4M1 ; MCM7
0.925 0.120 7 100103553 intron variant G/A snv 0.56 0.46 2
rs999788
IL10RB ; IL10RB-DT ; IFNAR2
0.925 0.120 21 33265726 non coding transcript exon variant C/T snv 0.20 2
rs9997745
ACSL1
0.925 0.040 4 184816689 intron variant G/A snv 0.25 2
rs999737
RAD51B
0.776 0.200 14 68567965 intron variant C/T snv 0.16 7
rs999716
SLC4A1
1.000 0.160 17 44262056 non coding transcript exon variant C/G;T snv 1
rs9996584
LOC107986229
4 74556244 intron variant A/G snv 0.59 1
rs9995
NBN ; OSGIN2
1.000 0.040 8 89933828 3 prime UTR variant A/G snv 0.32 1
rs999383
GRID1
1.000 0.040 10 86200054 intron variant C/T snv 0.42 1
rs9991821
SCARB2
1.000 0.040 4 76209132 intron variant G/A snv 0.18 1
rs9990999
DCTD
0.925 0.040 4 182902820 intron variant G/A snv 0.37 2
rs9990174
SLC6A1
1.000 0.040 3 10998753 intron variant G/T snv 0.31 2
rs9990
ADO
1.000 0.040 10 62808178 3 prime UTR variant C/T snv 0.23 1
rs9989661
LMTK3
0.925 0.080 19 48510834 intron variant T/C snv 0.21 2
rs9989419 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 1
rs9989407 16 68730609 intergenic variant C/A;G;T snv 1
rs9986765
PIP
0.925 0.120 7 143138146 intron variant A/G snv 0.12 2
rs9986517
CPNE5
1.000 0.080 6 36751302 intron variant C/A;T snv 1
rs998592
CLEC16A
0.925 0.160 16 11105821 intron variant C/T snv 0.39 1
rs9983925
ADARB1
21 45216929 intron variant C/T snv 0.46 4
rs998382
DNMT3B
1.000 0.040 20 32796330 intron variant A/G snv 0.49 1
rs9982601 0.851 0.080 21 34226827 intron variant C/T snv 0.15 2