Source: CURATED ×
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
rs78378222
TP53
0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 17
rs35446936
ACTRT3
0.776 0.080 3 169768720 intron variant G/A snv 0.21 11
rs12638862 0.827 0.160 3 169759718 downstream gene variant A/G snv 0.24 10
rs11031006
LOC105376607
0.882 0.120 11 30204981 intron variant G/A snv 0.11 7
rs2853676
TERT
0.667 0.560 5 1288432 intron variant T/A;C snv 7
rs121913121
FH
0.851 0.320 1 241513661 missense variant T/G snv 6
rs16991615
MCM8
0.925 0.080 20 5967581 missense variant G/A snv 4.5E-02 4.2E-02 6
rs7907606 0.790 0.120 10 103920874 upstream gene variant T/G snv 0.26 5
rs9419958
STN1
0.851 0.040 10 103916188 intron variant T/C snv 0.75 5
rs72709458
TERT
0.882 0.040 5 1283640 intron variant C/A;T snv 5
rs1800057
ATM
0.776 0.200 11 108272729 missense variant C/A;G snv 1.7E-02 4
rs1060499630
FH
0.882 0.320 1 241513659 stop gained G/A snv 4
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 4
rs11031731 0.925 0.040 11 32343884 upstream gene variant G/A snv 0.18 3
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 3
rs10917151
CDC42
0.925 0.040 1 22096228 3 prime UTR variant G/A snv 0.14 3
rs138420351
DNAH2
1.000 17 7796745 intron variant C/T snv 9.6E-03 3
rs2131371
LOC100288798
1.000 12 46402739 intron variant A/C snv 0.77 3
rs4335411
PGBD2
1.000 1 248897507 regulatory region variant G/A snv 0.82 3
rs6901631
SYNE1
1.000 6 152245912 intron variant T/A;C snv 3
rs71575922
SYNE1
0.925 0.040 6 152232879 intron variant C/G snv 0.12 3
rs12037376
WNT4
0.925 0.040 1 22135618 intron variant G/A snv 0.13 3
rs10508765 1.000 10 31679855 intergenic variant A/G snv 0.20 2
rs10835889 1.000 11 32348834 intergenic variant G/A snv 0.21 2