Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17458086
SLC2A13
0.925 0.120 12 40034837 intron variant T/C snv 1.1E-02 2
rs1810205
CUBN
0.925 0.120 10 16923228 intron variant A/G snv 0.47 2
rs2073389
SMARCB1
0.925 0.120 22 23791306 intron variant C/T snv 0.59 2
rs2255280
C9 ; DAB2
0.925 0.120 5 39394887 intron variant C/A snv 0.98 2
rs2457571
SLC22A3
0.925 0.120 6 160413796 intron variant T/C snv 0.62 2
rs2470353
XPC ; LOC107986063
0.925 0.120 3 14148768 intron variant G/A;C;T snv 0.41; 1.5E-04 2
rs2980874
TRIB1
0.925 0.120 8 125432546 intron variant G/A snv 0.30 2
rs3124761
SLC2A6
0.925 0.120 9 133474633 intron variant T/C snv 0.80 2
rs34852782
PRKAG2
0.925 0.120 7 151869086 intron variant -/A;AG ins 2
rs3729587
XPC
0.925 0.120 3 14167125 intron variant G/C snv 0.31 0.34 2
rs3731055
XPC ; LSM3
0.925 0.120 3 14178939 intron variant C/T snv 1.9E-02 2
rs3731114
XPC
0.925 0.120 3 14165122 intron variant C/G snv 1.8E-02 2
rs4795218
HNF1B ; LOC105371754
0.925 0.120 17 37718512 intron variant A/G snv 0.82 2
rs4927850
TFRC
0.925 0.120 3 196024759 intron variant T/C snv 0.71 2
rs5757573
PDGFB
0.925 0.120 22 39237617 intron variant C/T snv 0.57 2
rs5768709
TAFA5
0.925 0.120 22 48533757 intron variant A/G snv 0.36 2
rs6001516 0.925 0.120 22 39248198 intron variant C/T snv 6.1E-02 2
rs6127119
CYP24A1
0.925 0.120 20 54162543 intron variant C/T snv 0.24 2
rs62068300
RPTOR
0.925 0.120 17 80600927 intron variant G/A;T snv 5.7E-05 2
rs6464375
DPP6
0.925 0.120 7 153928758 intron variant C/T snv 6.7E-02 2
rs6475609
CDKN2B-AS1
0.925 0.120 9 22106272 intron variant A/C;G;T snv 2
rs708224
BICD1
0.925 0.120 12 32283475 intron variant A/G snv 0.50 2
rs78417682
TNS3
0.925 0.120 7 47449305 intron variant G/C snv 0.15 2
rs876493
PNMT
0.925 0.160 17 39668292 intron variant G/A snv 0.47 2
rs9854771
TP63
0.925 0.240 3 189790682 intron variant G/A snv 0.34 2