Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2074898
NDUFS7
1.000 0.040 19 1391362 intron variant A/C;G snv 3
rs2400707
ADRB2
1.000 0.040 5 148825489 5 prime UTR variant A/G;T snv 3
rs3915512
DLG1 ; MIR4797
1.000 0.040 3 197295369 intron variant A/G;T snv 3
rs9296158
FKBP5 ; LOC112267956
0.763 0.080 6 35599305 intron variant A/G snv 0.65 16
rs9470080
FKBP5
0.827 0.080 6 35678658 intron variant T/A;C snv 13
rs279858
GABRA2
0.851 0.080 4 46312576 synonymous variant T/C snv 0.40 0.38 8
rs669
A2M ; KLRG1
0.851 0.080 12 9079672 missense variant T/C snv 0.31 0.33 7
rs1561515242
CAMK4
1.000 0.080 5 111482938 splice donor variant G/A snv 6
rs12936511
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
0.925 0.080 17 45807036 synonymous variant C/T snv 3.1E-02 3.0E-02 5
rs279871
GABRA2
0.882 0.080 4 46303716 intron variant T/C snv 0.38 5
rs104894127
TPM2
0.925 0.080 9 35685750 missense variant G/C snv 4
rs121918805
LOC102724058 ; SCN1A-AS1 ; SCN1A
0.925 0.080 2 166002660 missense variant C/A;T snv 2.0E-05 4
rs2144025
ESR1
0.925 0.080 6 151986571 intron variant T/A;C snv 4
rs279826
GABRA2
1.000 0.080 4 46332192 intron variant A/G snv 0.46 4
rs137853208
FIGNL1 ; DDC
0.925 0.080 7 50504025 missense variant G/A snv 3
rs373288445
DISC1 ; TSNAX-DISC1
0.925 0.080 1 231694534 missense variant C/T snv 5.6E-05 4.2E-05 3
rs773758385
DISC1 ; TSNAX-DISC1
0.925 0.080 1 231694162 missense variant C/T snv 1.0E-04 3.5E-05 3
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs63751438
MAPT
0.776 0.120 17 46010388 missense variant C/T snv 16
rs6994992
NRG1
0.790 0.120 8 31638065 upstream gene variant C/A;T snv 13
rs2710102
CNTNAP2
0.790 0.120 7 147877298 intron variant A/G;T snv 12
rs27072
SLC6A3
0.807 0.120 5 1394407 3 prime UTR variant C/A;T snv 11
rs28936379
PSEN2
0.807 0.120 1 226888977 missense variant A/C;G;T snv 4.0E-06 10
rs2069845
IL6
0.807 0.120 7 22730530 intron variant G/A snv 0.61 8
rs121909671
FUS
0.851 0.120 16 31191419 missense variant G/A;T snv 4.0E-06 6