Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7182853
MAP2K1
1.000 0.040 15 66469947 intron variant T/C snv 0.31 1
rs12256138
SLC29A3
1.000 0.040 10 71336479 intron variant C/G;T snv 1
rs11240
CLOCK ; TMEM165
0.925 0.080 4 55453183 3 prime UTR variant C/A;G snv 2
rs1003880422
TH
0.925 0.080 11 2166716 missense variant G/A;T snv 6.9E-06 2
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
rs2412646
CLOCK ; TMEM165
0.882 0.120 4 55452605 3 prime UTR variant T/C snv 0.58 3
rs174696
COMT
0.925 0.080 22 19965653 intron variant C/A;T snv 3
rs242939
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
0.882 0.120 17 45818213 intron variant C/T snv 0.86 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
rs1432441
MAP2K1
0.882 0.040 15 66426943 intron variant G/A snv 0.27 3
rs1549854
MAP2K1
0.882 0.040 15 66404397 intron variant A/C;G snv 0.44 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