Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35705950 0.763 0.240 11 1219991 splice region variant G/A;T snv 14
rs623011 0.827 0.320 17 70263305 intergenic variant A/G snv 0.74 5
rs945270 0.925 0.040 14 55733755 intergenic variant C/G;T snv 3
rs757196717
ADRA1A
0.925 0.040 8 26770273 missense variant C/G;T snv 4.0E-06 2
rs767958027
ADRA2B
0.925 0.040 2 96114892 missense variant A/T snv 2
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs4930199
AIP
0.851 0.120 11 67490920 missense variant G/A;C snv 4
rs145047094
AIP
0.882 0.160 11 67483205 missense variant G/A snv 2.0E-03 1.9E-03 3
rs641081
AIP ; MIR6752
0.851 0.120 11 67490352 missense variant C/A snv 0.96 0.84 4
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs1800497
ANKK1
0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs587777741
ANLN
0.925 7 36411062 missense variant C/T snv 1.7E-05 3.5E-05 2
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs1801155
APC
0.649 0.440 5 112839514 missense variant T/A snv 8.0E-06; 2.0E-03 1.2E-03 42
rs1463038513
APC
0.658 0.440 5 112839511 frameshift variant TAAA/- delins 36
rs1801166
APC
0.732 0.200 5 112839543 missense variant G/C snv 4.4E-03 5.6E-03 17
rs5742904
APOB
0.689 0.280 2 21006288 missense variant C/A;T snv 2.8E-04 7.3E-04 22
rs12713559
APOB
0.776 0.120 2 21006196 missense variant G/A snv 3.4E-04 5.0E-04 10
rs144467873
APOB
0.776 0.120 2 21006289 missense variant G/A snv 1.7E-04 6.3E-05 9
rs63750264
APP
0.716 0.360 21 25891784 missense variant C/A;G;T snv 17
rs572842823
APP
0.763 0.160 21 25897626 missense variant T/A;G snv 11
rs371425292
APP
0.763 0.160 21 25897627 missense variant C/A;T snv 8.0E-06 10
rs950592627
APP
0.827 0.200 21 26090015 missense variant G/C snv 7.0E-06 5
rs763852444
APP
0.882 0.120 21 26112127 missense variant G/C snv 4.0E-06 3
rs200074159
APP
0.925 0.080 21 26000036 missense variant T/C snv 2.8E-05 5.6E-05 2