Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11466285
TGFA
0.851 0.200 2 70450307 3 prime UTR variant A/C;G snv 5
rs3771523
TGFA
0.851 0.200 2 70450336 3 prime UTR variant C/T snv 0.14 5
rs1487309678
SEMA3A
0.851 0.280 7 84014246 missense variant C/T snv 8.0E-06 5
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
rs12543318 0.882 0.120 8 87856112 intergenic variant C/A snv 0.68 4
rs7650466
EPHA3
0.851 0.200 3 89481208 3 prime UTR variant C/T snv 0.23 7
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
rs572007403
KISS1R
0.882 0.200 19 919955 missense variant C/A snv 3.3E-04 9.1E-05 4
rs560426
ABCA4
0.851 0.200 1 94087882 intron variant C/T snv 0.53 5
rs7043516
FOXE1
1.000 0.080 9 97855151 3 prime UTR variant A/C;T snv 2