Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 17
rs7705526
TERT
0.776 0.240 5 1285859 intron variant C/A;T snv 15
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 13
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 10
rs3117582
BAG6 ; APOM
0.716 0.440 6 31652743 intron variant T/G snv 7.1E-02 8
rs56113850
CYP2A6
0.807 0.080 19 40847202 intron variant T/C snv 0.52 8
rs1470579
IGF2BP2
0.925 0.160 3 185811292 intron variant A/C snv 0.46 4
rs4402960
IGF2BP2
0.724 0.400 3 185793899 intron variant G/T snv 0.38 4
rs667282
CHRNA5
0.790 0.120 15 78571130 intron variant T/C snv 0.28 4
rs7086803
VTI1A
0.763 0.160 10 112738717 intron variant G/A snv 0.20 4
rs744166
STAT3
0.689 0.560 17 42362183 intron variant A/G snv 0.48 4
rs3114020
ABCG2
0.882 0.200 4 88162514 intron variant T/C snv 0.40 3
rs7741164
FOXP4-AS1
0.882 0.080 6 41525674 intron variant G/A snv 6.6E-02 3
rs1200399
BAZ1A
0.925 0.080 14 34823979 intron variant C/T snv 0.87 2
rs16950650
ABCC4
1.000 0.080 13 95123178 intron variant C/T snv 4.7E-02 2
rs17635492 1.000 0.080 6 117450114 intron variant A/T snv 2.4E-02 2
rs314276
LIN28B
0.807 0.280 6 104960124 intron variant A/C snv 0.65 2
rs3769821
CASP8
0.851 0.200 2 201258707 intron variant C/T snv 0.57 2
rs4236709
NRG1
0.925 0.080 8 32552592 intron variant G/A;T snv 2
rs4488809
TP63
0.827 0.080 3 189638472 intron variant T/C snv 0.45 2
rs55768116
MPZL3
0.925 0.080 11 118237616 intron variant C/A snv 0.38 2
rs9651118
MTHFR
0.683 0.480 1 11802157 intron variant T/C snv 0.18 2
rs10023113
CAMK2D
1.000 0.080 4 113625548 intron variant A/G snv 0.18 1
rs1077424
DAB1
1.000 0.080 1 57344632 intron variant G/C snv 0.52 1
rs10937405
TP63
0.807 0.080 3 189665394 intron variant C/T snv 0.38 1