Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6598008
CDHR5
0.925 0.080 11 618172 intron variant A/G snv 0.48 2
rs4837766
CDK5RAP2
0.925 0.080 9 120402006 intron variant A/C;G;T snv 2
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
rs9331888
CLU ; MIR6843
0.827 0.200 8 27611345 5 prime UTR variant C/G snv 0.35 0.28 5
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs111943087
CSF1R
0.925 0.080 5 150059725 missense variant G/A snv 1.4E-05 2
rs754203
CYP46A1
0.807 0.200 14 99691630 non coding transcript exon variant A/G snv 0.27 6
rs11887120
DNMT3A
0.882 0.080 2 25262866 intron variant C/T snv 0.45 4
rs7354779
DNMT3L ; DNMT3L-AS1
0.827 0.200 21 44250887 missense variant T/C snv 0.21 6
rs11767557
EPHA1-AS1
0.882 0.080 7 143412046 intron variant T/C snv 0.18 4
rs9340803
ESR1
0.925 0.080 6 151842832 intron variant A/G snv 1.0E-03 3.8E-04 2
rs1256049
ESR2
0.645 0.560 14 64257333 synonymous variant C/T snv 6.7E-02 6.3E-02 32
rs2230288
GBA
0.776 0.160 1 155236376 missense variant C/T snv 1.0E-02 1.0E-02 18
rs4684677
GHRLOS ; GHRL
0.742 0.360 3 10286769 missense variant T/A snv 0.10 6.6E-02 13
rs7483
GSTM3 ; GSTM5
0.742 0.320 1 109737079 missense variant C/T snv 4.0E-06; 0.35 0.26 11
rs1130399
HLA-DQB1
1.000 0.040 6 32661978 missense variant G/A;T snv 0.20 1
rs35445101
HLA-DRB1
0.925 0.080 6 32579102 missense variant A/G snv 4.2E-04 2.7E-02 2
rs3846662
HMGCR
0.763 0.280 5 75355259 non coding transcript exon variant A/G snv 0.50 0.58 12
rs6313
HTR2A
0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs972936
IGF1 ; LINC02456
0.807 0.200 12 102431143 intron variant T/C snv 0.70 12
rs12053868
IL1RAP
0.925 0.080 3 190582215 intron variant A/G snv 8.0E-02 2
rs1207568
KL
0.925 0.120 13 33016046 upstream gene variant G/A snv 0.17 3
rs9527025
KL
1.000 0.040 13 33054056 missense variant G/C;T snv 0.14 1
rs8702
KLC1
0.851 0.160 14 103686015 3 prime UTR variant C/G snv 0.61 5
rs6850306
LCORL
0.925 0.080 4 18004466 intron variant G/A snv 0.12 2