Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10223646
rs10223646
DSE
4 0.882 0.080 6 116296236 intron variant C/T snv 0.41 0.010 1.000 1 2020 2020
dbSNP: rs1033656351
rs1033656351
P2RX4
7 0.827 0.160 12 121232997 missense variant G/A snv 1.6E-05 2.8E-05 0.010 1.000 1 2019 2019
dbSNP: rs10997871
rs10997871
SIRT1
3 0.925 0.080 10 67913178 intron variant T/C snv 4.1E-03 0.010 1.000 1 2019 2019
dbSNP: rs10997875
rs10997875 		4 0.882 0.080 10 67920067 downstream gene variant T/A;C snv 0.010 1.000 1 2019 2019
dbSNP: rs1402757753
rs1402757753
P2RX2
4 0.882 0.080 12 132621913 missense variant G/A snv 7.0E-06 0.010 1.000 1 2019 2019
dbSNP: rs1409851868
rs1409851868
EPHA3
6 0.882 0.080 3 89399325 missense variant A/G snv 0.010 1.000 1 2019 2019
dbSNP: rs1718119
rs1718119
P2RX7 ; LOC105370032
21 0.689 0.520 12 121177300 missense variant G/A;T snv 0.35; 4.0E-06 0.010 1.000 1 2019 2019
dbSNP: rs1743963
rs1743963
SGK1
4 0.882 0.120 6 134176537 intron variant G/A;C snv 0.010 1.000 1 2019 2019
dbSNP: rs174696
rs174696
COMT
3 0.925 0.080 22 19965653 intron variant C/A;T snv 0.010 1.000 1 2019 2019
dbSNP: rs1763509
rs1763509
SGK1
4 0.882 0.120 6 134233200 intron variant G/A;T snv 0.010 1.000 1 2019 2019
dbSNP: rs1800629
rs1800629
TNF
169 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2019 2019
dbSNP: rs1800947
rs1800947
CRP
28 0.683 0.440 1 159713648 splice region variant C/A;G;T snv 4.4E-05; 5.1E-02; 4.0E-06 0.010 1.000 1 2019 2019
dbSNP: rs2298383
rs2298383
ADORA2A ; ADORA2A-AS1 ; SPECC1L-ADORA2A
11 0.827 0.200 22 24429543 non coding transcript exon variant C/A;T snv 0.010 1.000 1 2019 2019
dbSNP: rs2470152
rs2470152
CYP19A1
6 0.827 0.240 15 51302775 intron variant G/A snv 0.50 0.010 1.000 1 2019 2019
dbSNP: rs2794521
rs2794521
CRP
15 0.742 0.480 1 159715306 upstream gene variant C/T snv 0.78 0.010 1.000 1 2019 2019
dbSNP: rs3125
rs3125
HTR2A
4 0.925 0.080 13 46834716 3 prime UTR variant C/G;T snv 0.010 1.000 1 2019 2019
dbSNP: rs4580704
rs4580704
CLOCK
13 0.790 0.200 4 55460540 intron variant G/C snv 0.69 0.010 1.000 1 2019 2019
dbSNP: rs4713916
rs4713916
FKBP5
11 0.790 0.160 6 35702206 intron variant A/C;G;T snv 0.010 1.000 1 2019 2019
dbSNP: rs6280
rs6280
DRD3
57 0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 0.010 1.000 1 2019 2019
dbSNP: rs755302767
rs755302767
P2RX2
4 0.882 0.080 12 132621835 missense variant G/A snv 4.0E-06 0.010 1.000 1 2019 2019
dbSNP: rs9376026
rs9376026
SGK1
3 0.925 0.080 6 134281316 intron variant T/C snv 0.43 0.010 1.000 1 2019 2019
dbSNP: rs9389154
rs9389154
SGK1
4 0.882 0.120 6 134293623 intron variant G/A snv 0.11 0.010 1.000 1 2019 2019
dbSNP: rs3800373
rs3800373
FKBP5 ; LOC101929309
22 0.752 0.200 6 35574699 3 prime UTR variant C/A snv 0.68 0.020 1.000 2 2018 2019
dbSNP: rs9470080
rs9470080
FKBP5
13 0.827 0.080 6 35678658 intron variant T/A;C snv 0.020 1.000 2 2018 2019
dbSNP: rs10514299
rs10514299
TMEM161B-AS1
6 0.827 0.120 5 88367793 intron variant C/T snv 0.21 0.010 1.000 1 2018 2018