Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10130587
BMP4
0.851 0.200 14 53952392 intron variant G/C snv 0.45 5
rs16260
CDH1
0.716 0.440 16 68737131 upstream gene variant C/A snv 0.24 19
rs1546124
CRISPLD2
0.807 0.200 16 84838445 5 prime UTR variant G/A;C snv 8.6E-06; 0.67 7
rs4783099
CRISPLD2
0.827 0.200 16 84907723 3 prime UTR variant C/T snv 0.37 6
rs2239907
SARM1 ; SLC46A1
0.851 0.200 17 28398728 3 prime UTR variant T/C snv 0.53 5
rs739439
SLC46A1 ; SARM1
0.851 0.200 17 28396803 3 prime UTR variant C/T snv 0.13 5
rs4791774
NTN1
0.882 0.240 17 9028802 intron variant A/C;G snv 4
rs4791331
NTN1
0.925 0.120 17 9028765 intron variant C/T snv 0.53 3
rs572007403
KISS1R
0.882 0.200 19 919955 missense variant C/A snv 3.3E-04 9.1E-05 4
rs13041247
LOC102724968
0.851 0.200 20 40640434 regulatory region variant T/C snv 0.36 5
rs2269529
MYH9 ; MIR6819
0.851 0.200 22 36288308 missense variant T/C snv 0.26 0.18 5
rs886039813
OFD1
0.827 0.160 X 13756600 frameshift variant C/- delins 8