Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs190853081
APOE
0.925 0.080 19 44909083 missense variant G/A snv 2.0E-04 5.6E-05 3
rs1335550286
APOE
1.000 0.040 19 44909005 missense variant G/A snv 7.0E-06 2
rs2074755
BAZ1B
0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 20
rs6929846
BTN2A1
0.827 0.160 6 26458037 5 prime UTR variant T/C snv 0.70 10
rs10790162
BUD13
0.882 0.160 11 116768388 intron variant A/G;T snv 0.93 7
rs2187126
BUD13
11 116765068 intron variant A/G snv 4.8E-02 2
rs3825041
BUD13
11 116760991 intron variant T/A;C snv 0.89 2
rs1169313
C12orf43
12 121004867 intron variant T/A;C snv 6
rs1169310
C12orf43 ; HNF1A
12 121001630 3 prime UTR variant G/A snv 0.31 3
rs2250656
C3
0.882 0.160 19 6718523 intron variant T/C snv 0.25 4
rs1042636
CASR
0.672 0.360 3 122284922 missense variant A/G snv 0.15 9.0E-02 23
rs11773845
CAV1
0.925 0.120 7 116551247 intron variant C/A snv 0.53 4
rs4580704
CLOCK
0.790 0.200 4 55460540 intron variant G/C snv 0.69 13
rs11932595
CLOCK
0.827 0.160 4 55457430 intron variant A/G;T snv 12
rs1801260
CLOCK ; TMEM165
0.695 0.280 4 55435202 3 prime UTR variant A/G snv 0.25 28
rs1414423445
CREB3L3
19 4171402 stop gained C/A;T snv 4.0E-06; 4.0E-06 1
rs912378886
CREB3L3
19 4155009 stop gained G/A snv 1.6E-05 1.4E-05 1
rs11635252
CRTC3
0.925 0.080 15 90528542 upstream gene variant T/C snv 0.88 4
rs3862434
CRTC3
1.000 0.080 15 90537155 intron variant A/G snv 0.48 3
rs11576175
CTSS
1.000 1 150754918 intron variant G/A snv 7.2E-02 2
rs1168013
DOCK7
1.000 0.120 1 62531167 intron variant C/G;T snv 6
rs10889332
DOCK7
1.000 0.120 1 62485187 3 prime UTR variant C/T snv 0.39 4
rs2808607
EGLN1
1.000 0.080 1 231405228 intron variant G/A snv 0.56 2
rs324420
FAAH
0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 36