Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs75629841
MTSS1
1.000 0.080 8 124714135 intron variant G/A;T snv 2
rs751093906
SLC20A2
0.882 0.200 8 42472255 stop gained G/A;C snv 4.0E-06 8
rs749924
LINC01880
2 242084344 upstream gene variant C/T snv 0.25 1
rs74910095 1.000 0.080 5 63545132 intergenic variant T/A snv 3.7E-02 2
rs74570061
ARL9
1.000 0.080 4 56517605 intron variant T/C snv 3.9E-02 2
rs7442201
NSG1
1.000 0.080 4 4360022 intron variant A/C;G snv 2
rs74155456 1.000 0.080 10 61070020 intergenic variant T/C snv 2.3E-02 2
rs741013
PRICKLE2
3 64306961 intron variant A/T snv 6.0E-02 1
rs7341791
CDKN2B-AS1
9 22112428 intron variant A/G snv 0.65 1
rs7341786
CDKN2B-AS1
9 22112242 intron variant A/C snv 0.65 2
rs73169578 1.000 0.080 13 21120420 intergenic variant G/A snv 3.1E-02 2
rs72928364
ABI3BP
1.000 0.080 3 100894935 intron variant C/T snv 0.39 2
rs712964 22 19168604 upstream gene variant T/C snv 0.66 2
rs7092929
LOC105376360 ; LINC02669
10 3496602 splice region variant A/C;T snv 1
rs7049105
CDKN2B-AS1
0.807 0.120 9 22028802 intron variant A/G snv 0.58 7
rs7044859
CDKN2B-AS1
0.925 0.080 9 22018782 intron variant T/A snv 0.56 3
rs7030641
CDKN2B-AS1
1.000 0.040 9 22054041 intron variant C/T snv 0.72 2
rs7028570
CDKN2B-AS1
1.000 0.040 9 22048684 intron variant G/A snv 0.50 2
rs7028268
CDKN2B-AS1
1.000 0.040 9 22048415 intron variant G/A snv 0.32 2
rs7027950
CDKN2B-AS1
1.000 0.040 9 22048392 intron variant C/T snv 0.49 2
rs7027048
CDKN2B-AS1
1.000 0.040 9 22053710 intron variant A/G;T snv 2
rs6898559
ALDH7A1
1.000 0.080 5 126557237 intron variant G/A snv 0.66 2
rs679038
CDKN2B-AS1
1.000 0.040 9 22029081 intron variant G/A;T snv 2
rs6754498
LOC107985783
1.000 0.080 2 185953121 non coding transcript exon variant A/C;G;T snv 2
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 14