Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs12921862
AXIN1
0.763 0.200 16 331927 intron variant C/A snv 0.18 10
rs314276
LIN28B
0.807 0.280 6 104960124 intron variant A/C snv 0.65 10
rs7977932
LRRC43 ; IL31
0.763 0.320 12 122172836 intron variant C/G;T snv 10
rs11651755
HNF1B
0.763 0.160 17 37739849 intron variant T/C snv 0.52 9
rs4758680
LRRC43
0.763 0.320 12 122170805 intron variant T/A;G snv 9
rs1243180
MLLT10
0.790 0.160 10 21626690 intron variant T/A snv 0.23 7
rs17401966
KIF1B
0.790 0.280 1 10325413 intron variant A/G snv 0.24 7
rs370681
AXIN1
0.807 0.200 16 342461 intron variant C/T snv 0.48 6
rs7405776
HNF1B
0.807 0.120 17 37733029 intron variant G/A;C snv 6
rs757210
HNF1B
0.807 0.160 17 37736525 intron variant C/G;T snv 6
rs10088218
LINC00824
0.851 0.120 8 128531703 intron variant G/A snv 0.13 4
rs11782652
CHMP4C
0.851 0.120 8 81741409 intron variant A/G snv 6.6E-02 4
rs183211
LRRC37A2 ; NSF
0.882 0.160 17 46710944 intron variant G/A snv 0.28 0.30 4
rs67164370
RASSF2
0.851 0.120 20 4787830 intron variant -/AGGGACT ins 4
rs9909104
SHMT1
0.882 0.200 17 18344707 intron variant T/C snv 0.30 4
rs10260419
THSD7A
0.882 0.120 7 11524758 intron variant C/G snv 0.26 3
rs1649942
NRG3
0.925 0.120 10 82191935 intron variant G/A;C snv 3
rs2252673
INSR
0.882 0.120 19 7150407 intron variant C/G snv 0.75 3
rs74917072
UBE2F ; UBE2F-SCLY
0.882 0.120 2 238022053 intron variant G/A;T snv 3
rs7651446
TIPARP
0.882 0.120 3 156689208 intron variant G/T snv 7.9E-02 3
rs9303542
SKAP1
0.882 0.120 17 48334138 intron variant A/G snv 0.34 3
rs10017134
UGT2A2 ; UGT2A1
0.925 0.120 4 69591303 intron variant T/C snv 0.75 2
rs10788679
ARHGEF10L
0.925 0.120 1 17590467 intron variant A/G snv 0.59 2