Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs769455
APOE
0.827 0.120 19 44908783 missense variant C/T snv 1.4E-03 6.9E-03 8
rs387906567
APOE
0.882 0.200 19 44908774 missense variant C/G;T snv 6.3E-06 4
rs11542035
APOE
19 44908706 missense variant G/A snv 1.9E-05 2.8E-05 1
rs805297
BAG6 ; APOM
0.851 0.280 6 31654829 intron variant C/A snv 0.23 6
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs6929846
BTN2A1
0.827 0.160 6 26458037 5 prime UTR variant T/C snv 0.70 10
rs10488698
BUD13
1.000 0.040 11 116763231 missense variant G/A snv 6.4E-02 4.8E-02 2
rs2187126
BUD13
11 116765068 intron variant A/G snv 4.8E-02 2
rs10488699
BUD13
11 116761784 intron variant C/T snv 1.0E-01 1
rs2043211
CARD8
0.653 0.480 19 48234449 missense variant A/T snv 0.33 0.29 29
rs1801725
CASR
0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 39
rs11961407
CCHCR1
6 31154630 missense variant G/A snv 3.0E-03 1.3E-02 2
rs1984112
CD36
0.807 0.280 7 80613604 intron variant A/G snv 0.33 8
rs708272
CETP
0.708 0.440 16 56962376 intron variant G/A snv 0.42 0.38 24
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 18
rs711752
CETP
1.000 0.040 16 56962299 splice region variant G/A;C snv 10
rs4580704
CLOCK
0.790 0.200 4 55460540 intron variant G/C snv 0.69 13
rs1049353
CNR1
0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs4773144
COL4A1 ; COL4A2
0.827 0.080 13 110308365 intron variant A/G snv 0.42 7
rs1265538677
CPB2-AS1 ; CPB2
0.790 0.200 13 46055808 synonymous variant A/G snv 4.0E-06 10
rs3742264
CPB2 ; CPB2-AS1
0.742 0.400 13 46073959 missense variant C/T snv 0.31 0.35 17
rs3811381
CR1
0.763 0.240 1 207616743 missense variant C/A;G snv 8.0E-06; 0.24 11
rs7003945
DGAT1
8 144326802 5 prime UTR variant G/A;C snv 1
rs3060
DGAT2
11 75800527 3 prime UTR variant T/C snv 0.14 0.22 1