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
rs895520
NPAS2
0.689 0.320 2 100961475 intron variant G/A snv 0.35 23
rs10165970
NPAS2
0.708 0.320 2 100840527 intron variant G/A snv 0.16 18
rs10519097
RORA
0.708 0.320 15 60997989 intron variant C/T snv 0.13 18
rs11943456
TMEM165
0.708 0.320 4 55410167 intron variant T/C snv 0.42 18
rs12953717
SMAD7
0.724 0.240 18 48927559 intron variant C/T snv 0.36 18
rs17024869
NPAS2
0.708 0.320 2 100843581 intron variant T/C snv 8.3E-02 18
rs7581886
NPAS2
0.708 0.320 2 100964784 intron variant C/T snv 0.92 18
rs7705526
TERT
0.776 0.240 5 1285859 intron variant C/A;T snv 15
rs9514828
TNFSF13B
0.752 0.440 13 108269025 intron variant C/T snv 0.35 12
rs956572
BCL2
0.742 0.280 18 63153338 intron variant A/G snv 0.65 11
rs2293157
STAT5A
0.763 0.120 17 42300657 intron variant C/A;T snv 9
rs735665
GRAMD1B
0.776 0.280 11 123490689 intron variant G/A snv 0.15 8
rs11755724
RREB1
0.807 0.320 6 7118757 intron variant A/G;T snv 7
rs301
LPL
0.925 0.160 8 19959423 intron variant T/C snv 0.24 0.26 7
rs6877842
DROSHA ; C5orf22
0.807 0.320 5 31532531 intron variant G/C snv 0.16 7
rs210143
GGNBP1 ; BAK1
0.827 0.160 6 33579153 intron variant T/C snv 0.74 6
rs6449182
CD38
0.807 0.160 4 15778830 intron variant C/G snv 0.22 6
rs13397985
SP110 ; SP140
0.827 0.280 2 230226508 intron variant T/C;G snv 5
rs17483466
MIR4435-2HG ; ACOXL
0.827 0.280 2 111039881 intron variant A/G snv 0.15 5
rs2456449
CASC19 ; PCAT1
0.827 0.280 8 127180736 intron variant A/G snv 0.30 5
rs4459895
LPP
0.827 0.160 3 188236626 intron variant A/C snv 0.88 5
rs4985726
TNFRSF13B
0.925 0.120 17 16960324 intron variant C/G snv 0.11 5
rs926070
TSBP1-AS1 ; TSBP1
0.827 0.320 6 32289789 intron variant G/A snv 0.68 5
rs11715604
NCK1
0.851 0.160 3 136870707 intron variant A/G;T snv 4