Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2279744
MDM2
0.605 0.640 12 68808800 intron variant T/G snv 0.31 47
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 36
rs11568820
VDR
0.672 0.480 12 47908762 intron variant C/T snv 0.38 27
rs2853676
TERT
0.667 0.560 5 1288432 intron variant T/A;C snv 23
rs8034191
HYKK
0.695 0.440 15 78513681 intron variant T/C snv 0.27 19
rs767649
MIR155HG ; MIR155
0.695 0.480 21 25572410 intron variant T/A snv 7.5E-02 18
rs1412125
HMGB1
0.724 0.360 13 30467458 intron variant C/G;T snv 17
rs2069840
IL6 ; IL6-AS1
0.742 0.360 7 22728953 intron variant C/G snv 0.27 13
rs1535045
CD40
0.742 0.360 20 46119460 intron variant C/A;G;T snv 12
rs7977932
LRRC43 ; IL31
0.763 0.320 12 122172836 intron variant C/G;T snv 10
rs10937405
TP63
0.807 0.080 3 189665394 intron variant C/T snv 0.38 9
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv 8
rs3117582
BAG6 ; APOM
0.716 0.440 6 31652743 intron variant T/G snv 7.1E-02 8
rs31489
CLPTM1L
0.763 0.320 5 1342599 intron variant C/A snv 0.41 8
rs7086803
VTI1A
0.763 0.160 10 112738717 intron variant G/A snv 0.20 8
rs1011970
CDKN2B-AS1
0.677 0.320 9 22062135 intron variant G/T snv 0.23 6
rs2352028
GPC5
0.851 0.080 13 91792975 intron variant C/G;T snv 6
rs3816360
ARNTL
0.807 0.120 11 13346203 intron variant T/C snv 0.58 6
rs4513061
AGBL1
0.807 0.080 15 86428401 intron variant G/A;T snv 6
rs595961
AGO1
0.807 0.160 1 35902179 intron variant A/G snv 0.30 0.37 6
rs10213865
LOC105374724 ; IL7R
0.827 0.120 5 35857748 intron variant A/C;T snv 5
rs1026411
LOC105375751 ; PCAT1
0.827 0.080 8 127014165 intron variant G/A;C snv 0.25 5
rs12910984
CHRNA3
0.827 0.080 15 78599285 intron variant G/A;C;T snv 5
rs2131877
XXYLT1
0.827 0.080 3 195137645 intron variant G/A snv 0.20 5
rs2290035
ARNTL
0.827 0.160 11 13386224 intron variant T/A snv 0.46 5