Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13041247
LOC102724968
0.851 0.200 20 40640434 regulatory region variant T/C snv 0.36 5
rs12532
MSX1
0.790 0.200 4 4863419 3 prime UTR variant A/G snv 0.36 10
rs4783099
CRISPLD2
0.827 0.200 16 84907723 3 prime UTR variant C/T snv 0.37 6
rs11362
DEFB1
0.742 0.360 8 6877877 5 prime UTR variant C/T snv 0.43 0.40 13
rs17563
BMP4
0.790 0.320 14 53950804 stop lost A/G snv 0.45 0.44 8
rs10130587
BMP4
0.851 0.200 14 53952392 intron variant G/C snv 0.45 5
rs4791331
NTN1
0.925 0.120 17 9028765 intron variant C/T snv 0.53 3
rs560426
ABCA4
0.851 0.200 1 94087882 intron variant C/T snv 0.53 5
rs2239907
SARM1 ; SLC46A1
0.851 0.200 17 28398728 3 prime UTR variant T/C snv 0.53 5
rs12543318 0.882 0.120 8 87856112 intergenic variant C/A snv 0.68 4
rs493760
DROSHA
0.851 0.200 5 31436933 intron variant C/T snv 0.74 5
rs642961 0.732 0.440 1 209815925 intergenic variant A/G snv 0.84 14