Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1048943
CYP1A1
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs1058172
CYP2D6 ; NDUFA6-DT
0.882 0.080 22 42127526 missense variant C/G;T snv 4.4E-06; 9.2E-02 4
rs2285947
DNAH11
0.807 0.120 7 21544470 intron variant G/A snv 0.44 7
rs2424913
DNMT3B
0.708 0.440 20 32786453 intron variant C/T snv 0.56 0.53 18
rs3213173
E2F1
0.776 0.120 20 33677440 missense variant C/T snv 1.2E-03 5.1E-03 8
rs3213176
E2F1
0.776 0.120 20 33676869 missense variant C/T snv 1.9E-02; 5.1E-06 1.8E-02 8
rs763015080
EDNRA
0.851 0.120 4 147539821 missense variant G/A snv 4.1E-06 4
rs1051740
EPHX1
0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs2234922
EPHX1
0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 42
rs1799793
ERCC2
0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs759412116
ERCC2
0.581 0.640 19 45352210 missense variant C/G;T snv 4.0E-06; 6.0E-05 55
rs4150403
ERCC3
0.925 0.040 2 127292492 3 prime UTR variant C/T snv 5.7E-02 2
rs4253132
ERCC6
0.925 0.040 10 49493110 splice region variant G/A;T snv 0.89; 4.4E-05 2
rs10882272
FFAR4
0.925 0.040 10 93588425 3 prime UTR variant T/C snv 0.44 3
rs351855
FGFR4
0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 58
rs12212067
FOXO3
0.716 0.320 6 108659993 intron variant T/G snv 0.14 20
rs4946936
FOXO3
0.790 0.160 6 108682118 3 prime UTR variant T/A;C snv 8
rs6898743
GHR
0.776 0.160 5 42602390 intron variant C/G snv 0.78 9
rs1629816
GHRL ; GHRLOS ; SEC13
0.851 0.080 3 10294607 non coding transcript exon variant G/A;C snv 4
rs758272654
GNAS
0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs768623239
GSTM1 ; GSTM2
0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05 26
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1138272
GSTP1
0.611 0.600 11 67586108 missense variant C/T snv 5.9E-02 5.5E-02 42
rs770460061
GSTP1
0.742 0.240 11 67585239 missense variant T/C;G snv 4.0E-06; 1.2E-05 14
rs920778
HOTAIR
0.633 0.480 12 53966448 intron variant G/A snv 0.57 36