Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 19
rs121918130
INPP5E
0.716 0.360 9 136433182 missense variant G/A;T snv 3.4E-05; 4.2E-06 18
rs10936599
MYNN
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 18
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 16
rs7731626
ANKRD55
0.716 0.240 5 56148856 intron variant G/A snv 0.30 15
rs1563221666
SFTPC
0.882 0.120 8 22162694 missense variant C/T snv 14
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 12
rs12638862 0.827 0.160 3 169759718 downstream gene variant A/G snv 0.24 10
rs1990760
IFIH1
0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 10
rs2869966
LOC105377327 ; FAM13A
1.000 0.040 4 88947927 intron variant C/T snv 0.47 9
rs2869967
FAM13A ; LOC105377327
0.827 0.120 4 88948181 intron variant T/C snv 0.49 8
rs4072037
MUC1
0.732 0.240 1 155192276 splice acceptor variant C/A;T snv 0.59 7
rs2853676
TERT
0.667 0.560 5 1288432 intron variant T/A;C snv 7
rs7671167
FAM13A
0.925 0.040 4 88962828 intron variant C/T snv 0.53 6
rs393152
LINC02210 ; LINC02210-CRHR1
0.851 0.160 17 45641777 non coding transcript exon variant A/G snv 0.18 0.29 6
rs8070723
MAPT
0.851 0.240 17 46003698 intron variant A/G snv 0.18 6
rs12696304 0.776 0.320 3 169763483 downstream gene variant C/G snv 0.38 5
rs149989682
ABCA3
0.790 0.240 16 2317763 missense variant T/A;C snv 2.3E-03 5
rs2904259
FAM13A
4 88964563 intron variant T/A;C snv 5
rs2045517
LOC105377327 ; FAM13A
4 88949813 intron variant C/T snv 0.49 5
rs6793295
LRRC34
0.827 0.240 3 169800667 missense variant T/C;G snv 0.37; 1.8E-04 5
rs951005 0.807 0.200 9 34743684 intron variant G/A snv 0.78 4
rs2076295
DSP
0.882 0.080 6 7562999 intron variant T/G snv 0.46 4
rs1903003
FAM13A
0.925 0.080 4 88965146 intron variant C/G;T snv 4
rs10758593
GLIS3
0.827 0.240 9 4292083 intron variant G/A snv 0.45 4