Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2723341
NR2E3
0.807 0.160 15 71811481 splice acceptor variant A/C snv 5.3E-04 5.1E-04 8
rs28937873
NR2E3
0.807 0.160 15 71813573 missense variant G/A snv 4.0E-04 3.1E-04 7
rs1555454566
NR2E3
0.882 0.160 15 71811553 inframe deletion ACGGCTGCA/- delins 3
rs766096417
NR2E3
0.925 0.160 15 71811831 missense variant G/A snv 2.0E-05 7.0E-06 3
rs146403122
NR2E3
0.925 0.160 15 71811966 missense variant G/A snv 4.3E-03 1.8E-03 2
rs377257254
NR2E3
1.000 0.160 15 71813408 missense variant C/A;T snv 3.7E-05; 2.1E-05 2
rs781915220
OPN1LW
0.925 0.160 X 154150787 missense variant A/G snv 5.5E-06 2
rs1012493577
NR2E3
1.000 0.160 15 71811768 missense variant G/A snv 1.3E-05 2.8E-05 1
rs104894492
NR2E3
1.000 0.160 15 71811590 missense variant C/A;T snv 1.3E-05; 3.0E-05; 4.4E-06 2.8E-05 1
rs104894493
NR2E3
1.000 0.160 15 71811591 missense variant G/A snv 2.0E-04 3.1E-04 1
rs1278137915
NR2E3
1.000 0.160 15 71811783 missense variant G/A;T snv 1
rs1303613101
NR2E3
1.000 0.160 15 71817671 missense variant T/A;C snv 8.1E-06; 4.0E-06 1
rs1489149705
NR2E3
1.000 0.160 15 71811810 missense variant G/A snv 2.1E-05 1
rs1567159701
NR2E3
1.000 0.160 15 71811559 inframe deletion GCAGCGGCT/- delins 1
rs752883545
NR2E3
1.000 0.160 15 71814024 missense variant T/C snv 8.2E-06 7.0E-06 1
rs759629930
NR2E3
1.000 0.160 15 71814020 missense variant G/C snv 8.2E-06 1.4E-05 1
rs766769900
NR2E3
1.000 0.160 15 71817605 missense variant G/A;C snv 4.0E-06; 4.0E-06 1
rs774102273
NR2E3
1.000 0.160 15 71813566 missense variant C/G;T snv 4.1E-06; 8.2E-06 1
rs990307718
NR2E3
1.000 0.160 15 71811830 missense variant C/T snv 2.0E-05 7.0E-06 1
rs762991211
NRL
1.000 0.160 14 24082758 stop gained G/A snv 8.0E-06 1
rs779710488
NRL
1.000 0.160 14 24082491 missense variant C/T snv 8.1E-06 1