Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 31
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 19
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 17
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 16
rs2853676
TERT
0.667 0.560 5 1288432 intron variant T/A;C snv 7
rs380286
CLPTM1L
0.776 0.200 5 1320132 intron variant G/A snv 0.47 6
rs4635969 0.827 0.160 5 1308437 downstream gene variant G/A;T snv 5
rs4975616 0.763 0.320 5 1315545 downstream gene variant G/A snv 0.51 5
rs31489
CLPTM1L
0.763 0.320 5 1342599 intron variant C/A snv 0.41 5
rs995030
KITLG
0.776 0.320 12 88496894 3 prime UTR variant A/G snv 0.67 5
rs1508595 0.851 0.240 12 88592239 intron variant G/A;T snv 4
rs4624820 0.851 0.240 5 142302223 regulatory region variant G/A snv 0.55 4
rs2900333
ATF7IP
0.882 0.200 12 14500933 3 prime UTR variant C/A;G;T snv 4
rs31490
CLPTM1L
0.776 0.280 5 1344343 splice region variant G/A;T snv 0.37; 8.0E-06 4
rs755383
DMRT1
0.807 0.120 9 863635 intron variant C/T snv 0.54 4
rs210138
GGNBP1 ; BAK1
0.851 0.240 6 33574761 intron variant A/G snv 0.19 4
rs3782181
KITLG
0.882 0.120 12 88559784 intron variant C/A snv 0.65 4
rs4842610 1.000 0.120 12 88417912 intergenic variant C/T snv 0.56 2
rs421629
CLPTM1L
0.925 0.160 5 1320021 intron variant G/A snv 0.50 2
rs452932
CLPTM1L
0.925 0.160 5 1330138 intron variant T/C snv 0.46 2
rs467095
CLPTM1L
0.925 0.160 5 1336106 intron variant T/C snv 0.50 2
rs513349
GGNBP1 ; BAK1
1.000 0.120 6 33573942 intron variant A/G snv 0.51 0.51 2
rs11104896 1.000 0.120 12 88471464 regulatory region variant T/C snv 8.1E-02 1
rs11104901 1.000 0.120 12 88480402 intergenic variant G/T snv 7.9E-02 1
rs11167772 1.000 0.120 5 142276991 intergenic variant T/C snv 0.40 1