Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3821831
ITIH4
1.000 0.040 3 52819385 splice region variant C/T snv 0.29 0.29 2
rs736408
ITIH3
1.000 0.040 3 52801338 intron variant C/T snv 0.47 2
rs5522
NR3C2
0.732 0.320 4 148436323 missense variant C/T snv 0.88 0.89 19
rs11932595
CLOCK
0.827 0.160 4 55457430 intron variant A/G;T snv 12
rs112025902 0.925 0.080 4 120232669 intron variant A/G;T snv 4
rs1403522266
GABRB1
4 47320137 missense variant A/G snv 4.0E-06 1
rs713224
F11-AS1
4 186491213 intron variant G/A;C snv 1
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs41423247
NR3C1
0.695 0.440 5 143399010 intron variant G/C snv 0.31 23
rs6198
NR3C1
0.724 0.480 5 143278056 3 prime UTR variant T/C snv 0.12 16
rs33388
NR3C1
0.776 0.360 5 143317730 intron variant A/T snv 0.53 12
rs27072
SLC6A3
0.807 0.120 5 1394407 3 prime UTR variant C/A;T snv 11
rs686
DRD1
0.807 0.080 5 175441697 3 prime UTR variant G/A;C;T snv 9
rs6191
NR3C1
0.925 0.040 5 143278591 3 prime UTR variant C/A snv 0.48 4
rs10055255
CRHBP
1.000 0.040 5 76968168 intron variant A/T snv 0.50 2
rs161645
LOC105379109
1.000 0.040 5 104734216 intron variant A/G snv 0.77 2
rs10473984
CRHBP
5 76971301 intron variant G/T snv 0.12 1
rs3756290
RAPGEF6
5 131616057 intron variant A/G snv 0.56 1
rs4481363
LOC105377703
5 165047713 intron variant C/A snv 0.55 1
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs1360780
FKBP5 ; LOC112267956
0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs3800373
LOC101929309 ; FKBP5
0.752 0.200 6 35574699 3 prime UTR variant C/A snv 0.68 22
rs2229094
LOC100287329 ; LTA
0.776 0.320 6 31572779 missense variant T/C snv 0.27 0.27 17