Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4783099
CRISPLD2
0.827 0.200 16 84907723 3 prime UTR variant C/T snv 0.37 6
rs4791331
NTN1
0.925 0.120 17 9028765 intron variant C/T snv 0.53 3
rs4791774
NTN1
0.882 0.240 17 9028802 intron variant A/C;G snv 4
rs493760
DROSHA
0.851 0.200 5 31436933 intron variant C/T snv 0.74 5
rs560426
ABCA4
0.851 0.200 1 94087882 intron variant C/T snv 0.53 5
rs572007403
KISS1R
0.882 0.200 19 919955 missense variant C/A snv 3.3E-04 9.1E-05 4
rs642961 0.732 0.440 1 209815925 intergenic variant A/G snv 0.84 14
rs7043516
FOXE1
1.000 0.080 9 97855151 3 prime UTR variant A/C;T snv 2
rs739439
SLC46A1 ; SARM1
0.851 0.200 17 28396803 3 prime UTR variant C/T snv 0.13 5
rs7650466
EPHA3
0.851 0.200 3 89481208 3 prime UTR variant C/T snv 0.23 7
rs797044484
TP63
0.776 0.400 3 189868624 missense variant C/G snv 10
rs886039813
OFD1
0.827 0.160 X 13756600 frameshift variant C/- delins 8