Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799836
MAOB
0.790 0.160 X 43768752 intron variant T/A;C snv 0.43 7
rs2295633
FAAH
0.827 0.120 1 46408711 intron variant A/G;T snv 7
rs7225002
KANSL1
0.925 0.080 17 46111701 intron variant A/G snv 0.39 7
rs8070723
MAPT
0.851 0.240 17 46003698 intron variant A/G snv 0.18 7
rs1014290
SLC2A9 ; LOC105374476
0.827 0.280 4 10000237 intron variant G/A snv 0.72 6
rs10410544
SIRT2
0.827 0.120 19 38894892 intron variant T/C snv 0.68 0.67 6
rs1545843
LOC107984536
0.827 0.120 12 84170289 intron variant G/A snv 0.52 6
rs16976358
LINC00907
0.827 0.080 18 42611606 intron variant T/C snv 1.0E-02 6
rs1864325
MAPT
0.882 0.160 17 45900461 intron variant C/T snv 0.14 6
rs3129882
HLA-DRA
0.807 0.240 6 32441753 intron variant G/A snv 0.56 6
rs3794087
SLC1A2
0.851 0.120 11 35308068 intron variant G/T snv 0.20 6
rs4409766
BORCS7-ASMT ; BORCS7
1.000 0.040 10 102856906 intron variant T/C snv 0.14 6
rs588765
CHRNA5
0.827 0.200 15 78573083 intron variant T/A;C snv 6
rs8111699
STK11
0.851 0.200 19 1209715 intron variant C/G snv 0.53 6
rs11856808
LINGO1
0.827 0.120 15 77680428 intron variant C/T snv 0.42 5
rs132985
PLA2G6
0.827 0.120 22 38167464 intron variant C/T snv 0.51 5
rs2306604
TFAM
0.827 0.080 10 58388932 intron variant A/C;G;T snv 5
rs2435200
MAPT
0.925 0.080 17 45994485 intron variant G/A snv 0.40 5
rs34517613
KRT18P55
0.827 0.080 17 28283226 intron variant C/T snv 9.1E-02 5
rs3764435
ALDH1A1
0.827 0.120 9 72901960 intron variant A/C;T snv 5
rs3836790
SLC6A3
0.882 0.080 5 1411740 intron variant -/ACATACACACTCAGACACACATACCATGCA ins 5
rs40184
SLC6A3
0.851 0.120 5 1394962 intron variant C/T snv 0.45 5
rs4434553
TFR2
1.000 0.040 7 100642568 intron variant A/G snv 0.40 5
rs7224296
LRRC37A2 ; NSF
0.882 0.160 17 46722680 intron variant G/A snv 0.59 5
rs11724804
DGKQ
0.882 0.160 4 971991 intron variant G/A snv 0.43 4