Source: ALL
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 53
rs2853676
TERT
0.667 0.560 5 1288432 intron variant T/A;C snv 29
rs5029939
TNFAIP3
0.701 0.440 6 137874586 intron variant C/G snv 0.13 19
rs7731626
ANKRD55
0.716 0.240 5 56148856 intron variant G/A snv 0.30 16
rs2869967
FAM13A ; LOC105377327
0.827 0.120 4 88948181 intron variant T/C snv 0.49 11
rs10507391
ALOX5AP
0.776 0.320 13 30737959 intron variant A/T snv 0.52 10
rs951005 0.807 0.200 9 34743684 intron variant G/A snv 0.78 10
rs2280883
FOXP3
0.827 0.280 X 49252667 intron variant T/C snv 0.30 9
rs2869966
LOC105377327 ; FAM13A
1.000 0.040 4 88947927 intron variant C/T snv 0.47 9
rs10758593
GLIS3
0.827 0.240 9 4292083 intron variant G/A snv 0.45 8
rs7671167
FAM13A
0.925 0.040 4 88962828 intron variant C/T snv 0.53 7
rs8070723
MAPT
0.851 0.240 17 46003698 intron variant A/G snv 0.18 7
rs2045517
LOC105377327 ; FAM13A
4 88949813 intron variant C/T snv 0.49 5
rs2076295
DSP
0.882 0.080 6 7562999 intron variant T/G snv 0.46 5
rs2904259
FAM13A
4 88964563 intron variant T/A;C snv 5
rs17563986
MAPT
1.000 0.040 17 45913906 intron variant A/G snv 0.14 4
rs1903003
FAM13A
0.925 0.080 4 88965146 intron variant C/G;T snv 4
rs2609255
FAM13A
0.882 0.080 4 88890044 intron variant G/T snv 0.73 4
rs2853672
TERT
0.882 0.080 5 1292868 intron variant C/A;G snv 4
rs3793964
TOLLIP
0.882 0.120 11 1280752 intron variant T/C snv 0.66 4
rs546433642
KANSL1
0.925 0.120 17 46172742 intron variant T/C;G snv 4
rs549599956
KANSL1
0.925 0.120 17 46169798 intron variant A/G snv 4
rs7020673
GLIS3
0.882 0.200 9 4291747 intron variant C/A;G snv 4
rs7572733
PLCL1
0.925 0.120 2 198065082 intron variant C/T snv 0.43 4
rs11191865
STN1
0.925 0.160 10 103913084 intron variant G/A snv 0.44 3