Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9603618 1.000 0.120 13 39797240 intergenic variant C/T snv 0.24 1
rs9603616 1.000 0.120 13 39793932 downstream gene variant C/T snv 0.30 1
rs9603612
COG6
0.925 0.120 13 39760715 intron variant C/G snv 0.30 2
rs9598783 1.000 0.120 13 64371042 TF binding site variant C/G snv 0.43 1
rs959728
PRKCH
1.000 0.120 14 61467300 intron variant C/T snv 0.72 1
rs9594987
ENOX1
1.000 0.120 13 43656858 intron variant T/C snv 0.44 1
rs957765 1.000 0.120 6 30174913 downstream gene variant G/A snv 0.17 1
rs9571178 1.000 0.120 13 64362111 intergenic variant G/A;T snv 1
rs9565072
KLF12
1.000 0.120 13 74065662 intergenic variant T/A;C snv 1
rs9562501
ENOX1
1.000 0.120 13 43631547 intron variant A/G snv 0.51 1
rs9557321
LOC101927437 ; CLYBL
1.000 0.120 13 99868847 intron variant T/C snv 3.8E-02 1
rs954905 1.000 0.120 18 77620551 upstream gene variant A/G;T snv 1
rs9533156
TNFSF11
0.807 0.280 13 42573535 intron variant T/C snv 0.47 8
rs953038635
SOD2
0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51
rs9516053
GPC5
1.000 0.120 13 92293631 intron variant T/A;C snv 1
rs951005 0.807 0.200 9 34743684 intron variant G/A snv 0.78 10
rs9501626 0.925 0.200 6 32432567 regulatory region variant C/A snv 0.18 2
rs948138
LOC101928477
1.000 0.120 11 102630934 downstream gene variant G/A snv 0.59 1
rs947474
LINC02649 ; LINC02656
0.827 0.440 10 6348488 intron variant G/A snv 0.79 5
rs9469583
IP6K3
1.000 0.120 6 33749993 upstream gene variant T/C snv 0.52 1
rs9469566
UQCC2
1.000 0.120 6 33699828 intron variant C/A snv 0.41 1
rs9469084
TNXB
1.000 0.120 6 32112606 non coding transcript exon variant C/T snv 0.12 1
rs9461799 0.807 0.360 6 32721752 downstream gene variant T/C snv 0.37 6
rs945635
FCRL3
0.882 0.200 1 157700500 5 prime UTR variant C/A;G snv 5.6E-05; 0.45 4
rs944796
CDKN2B-AS1
1.000 0.120 9 22115286 intron variant C/G snv 0.15 1