Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12708716
CLEC16A
0.807 0.320 16 11086016 intron variant A/G snv 0.37 7
rs1004446
IGF2 ; INS-IGF2 ; IGF2-AS
0.827 0.240 11 2148913 intron variant G/A snv 0.37 7
rs2927438 0.925 0.080 19 44738850 intergenic variant G/A snv 0.20 6
rs2965101 1.000 0.080 19 44734556 intergenic variant T/C snv 0.34 6
rs4788084
IL27
0.827 0.200 16 28528527 downstream gene variant C/T snv 0.36 6
rs11755527
BACH2
0.851 0.360 6 90248512 intron variant C/G snv 0.36 5
rs12722495
IL2RA
0.851 0.200 10 6055320 intron variant T/C snv 7.0E-02 5
rs1701704
LOC105369781 ; IKZF4
0.851 0.200 12 56018703 intron variant T/G snv 0.25 5
rs8106922
TOMM40
1.000 0.080 19 44898409 intron variant A/G snv 0.36 5
rs3788013
UBASH3A
0.851 0.240 21 42421219 intron variant C/A snv 0.44 5
rs4689388
WFS1
0.882 0.360 4 6268329 upstream gene variant G/A snv 0.64 4
rs543293 0.925 0.080 11 86109035 regulatory region variant A/G snv 0.72 3
rs4712523
CDKAL1
0.925 0.120 6 20657333 intron variant A/G snv 0.41 3
rs12518099
LINC01339
0.925 0.120 5 90250292 intron variant A/G;T snv 3
rs7171171
LOC107984725
0.925 0.120 15 38614840 intergenic variant A/G snv 0.24 3
rs428595
LOC107985532
1.000 0.120 22 21662102 non coding transcript exon variant A/G snv 0.98 3
rs3842727
TH
1.000 0.120 11 2163618 upstream gene variant G/T snv 0.58 3
rs11894266 1.000 0.080 2 169780132 downstream gene variant C/T snv 0.45 2
rs2582367 1.000 0.080 8 27622508 regulatory region variant C/T snv 0.64 2
rs8103315
BCL3
1.000 0.080 19 44750911 intron variant C/A snv 9.1E-02 2
rs3760627
CLPTM1
1.000 0.080 19 44953923 non coding transcript exon variant T/C snv 0.80 0.51 2
rs12610605
NECTIN2
1.000 0.080 19 44867581 intron variant G/A snv 0.15 2
rs1871047
NECTIN2
1.000 0.080 19 44848489 intron variant A/G snv 0.31 2
rs377702
NECTIN2
1.000 0.080 19 44859410 intron variant G/A snv 0.34 2
rs1048699
PPP1R37 ; MARK4
1.000 0.080 19 45147128 3 prime UTR variant C/T snv 9.0E-02 2