Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10510057 0.925 0.080 10 119551536 intergenic variant G/C snv 0.22 3
rs1937863
AKR1C2
0.925 0.080 10 5009340 intron variant G/A;C;T snv 3
rs33990840
AVPR1B
0.925 0.080 1 206116320 missense variant C/G;T snv 5.0E-02; 2.8E-05 3
rs139832701
CAV3
0.925 0.080 3 8773124 intron variant T/G snv 0.13 3
rs553040076
CDC37 ; PDE4A
0.925 0.080 19 10417700 missense variant T/A snv 4.5E-05 7.7E-05 3
rs174696
COMT
0.925 0.080 22 19965653 intron variant C/A;T snv 3
rs1935062
DAOA ; DAOA-AS1
0.882 0.080 13 105475787 intron variant A/C snv 0.32 3
rs4658966
DISC1 ; TSNAX-DISC1 ; DISC1-IT1
0.925 0.080 1 231942868 intron variant T/C snv 0.19 3
rs977605156
DNASE1 ; TRAP1
0.925 0.080 16 3656127 missense variant G/A snv 7.0E-06 3
rs747052707
FOLH1
0.925 0.080 11 49192822 missense variant T/C snv 2.4E-05; 8.1E-06 3
rs2133450
GRM7
0.925 0.080 3 7294765 intron variant A/C snv 0.38 3
rs6704393
NOS1AP
0.925 0.080 1 162182266 intron variant C/A;T snv 3
rs1187329
NTRK2
0.925 0.080 9 84674365 intron variant A/G snv 0.52 3
rs1364647619
POMC
0.925 0.080 2 25161334 missense variant C/T snv 3
rs9376026
SGK1
0.925 0.080 6 134281316 intron variant T/C snv 0.43 3
rs10997871
SIRT1
0.925 0.080 10 67913178 intron variant T/C snv 4.1E-03 3
rs5558
SLC6A2
0.925 0.080 16 55699647 missense variant T/G snv 3
rs8192625
TAAR6
0.925 0.080 6 132571193 missense variant G/A snv 6.2E-02 7.8E-02 3
rs7486220
TIMELESS
0.925 0.080 12 56443632 intron variant C/T snv 3
rs12229394
TPH2
0.925 0.080 12 71999134 intron variant G/A snv 0.29 3
rs12137417
TSNAX-DISC1 ; DISC1
0.925 0.080 1 231950407 intron variant G/A snv 0.17 3
rs2793094
TSNAX-DISC1 ; DISC1
0.925 0.080 1 231741236 intron variant G/A snv 0.97 3
rs10997875 0.882 0.080 10 67920067 downstream gene variant T/A;C snv 4
rs112025902 0.925 0.080 4 120232669 intron variant A/G;T snv 4
rs1491851 0.925 0.080 11 27731216 intron variant T/C;G snv 0.41 4