Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2269529
MYH9 ; MIR6819
0.851 0.200 22 36288308 missense variant T/C snv 0.26 0.18 5
rs3771523
TGFA
0.851 0.200 2 70450336 3 prime UTR variant C/T snv 0.14 5
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
rs739439
SLC46A1 ; SARM1
0.851 0.200 17 28396803 3 prime UTR variant C/T snv 0.13 5
rs12543318 0.882 0.120 8 87856112 intergenic variant C/A snv 0.68 4
rs4791774
NTN1
0.882 0.240 17 9028802 intron variant A/C;G snv 4
rs572007403
KISS1R
0.882 0.200 19 919955 missense variant C/A snv 3.3E-04 9.1E-05 4
rs4791331
NTN1
0.925 0.120 17 9028765 intron variant C/T snv 0.53 3
rs3775261
MSX1
1.000 0.080 4 4862018 intron variant C/A snv 0.30 2
rs3821949
MSX1
1.000 0.080 4 4858675 upstream gene variant G/A snv 0.32 2
rs7043516
FOXE1
1.000 0.080 9 97855151 3 prime UTR variant A/C;T snv 2