Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs9825823
FHIT
0.851 0.080 3 61096480 intron variant T/C snv 0.47 5
rs977605156
DNASE1 ; TRAP1
0.925 0.080 16 3656127 missense variant G/A snv 7.0E-06 3
rs9722
S100B
0.776 0.200 21 46599326 3 prime UTR variant G/A snv 0.16; 2.4E-05 0.21 9
rs9657182
IDO1
0.851 0.280 8 39908329 intron variant C/G;T snv 6
rs9470080
FKBP5
0.827 0.080 6 35678658 intron variant T/A;C snv 13
rs9389154
SGK1
0.882 0.120 6 134293623 intron variant G/A snv 0.11 4
rs9376026
SGK1
0.925 0.080 6 134281316 intron variant T/C snv 0.43 3
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs9296158
FKBP5 ; LOC112267956
0.763 0.080 6 35599305 intron variant A/G snv 0.65 16
rs908867 0.851 0.160 11 27724217 intron variant C/G;T snv 7
rs900418273
ANKK1
0.807 0.120 11 113393764 missense variant A/G snv 8
rs893924483
BDNF ; BDNF-AS
0.716 0.280 11 27658285 missense variant C/A;T snv 4.0E-06 1.4E-05 23
rs885479
MC1R
0.732 0.280 16 89919746 missense variant G/A snv 0.15 8.3E-02 16
rs884344
GDNF ; GDNF-AS1
0.882 0.120 5 37824138 intron variant A/C snv 0.33 5
rs8192625
TAAR6
0.925 0.080 6 132571193 missense variant G/A snv 6.2E-02 7.8E-02 3
rs80356704
CLCN1
0.827 0.200 7 143341938 missense variant C/T snv 4.4E-05 2.1E-05 6
rs7997012
HTR2A
0.807 0.080 13 46837850 intron variant A/G snv 0.69 11
rs797045032
CLCN1
0.827 0.280 7 143321720 missense variant GG/TC mnv 11
rs794727961
CACNA1C
0.851 0.080 12 2512979 missense variant G/A snv 5
rs78162420
TPH2
0.882 0.120 12 71941600 missense variant C/A snv 2.1E-03 7.1E-04 4
rs7813
GEMIN4
0.689 0.360 17 744946 missense variant G/A;C snv 0.63 22
rs776943620
ACE
0.851 0.120 17 63477287 missense variant G/A snv 2.1E-05 7
rs7766029 0.851 0.080 6 88137716 downstream gene variant T/C snv 0.51 7
rs772659997
CHAT
0.882 0.120 10 49619853 synonymous variant T/C snv 2.0E-05 4