Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1046943
MICAL1 ; ZBTB24
1.000 0.040 6 109462738 3 prime UTR variant A/G snv 0.52 3
rs11001178
KAT6B
1.000 0.040 10 74842047 intron variant T/C;G snv 1
rs11636988
GABRB3
1.000 0.040 15 26577667 intron variant G/A snv 0.43 1
rs11637898
ST8SIA2
0.925 0.040 15 92409620 intron variant G/A snv 0.43 2
rs11956731
GABRA6
1.000 0.040 5 161700816 intron variant C/A;T snv 1
rs1200746244
MTHFR
0.807 0.080 1 11801287 missense variant C/T snv 4.0E-06 7.0E-06 11
rs12547858
NRG1
1.000 0.040 8 32629535 intron variant C/T snv 0.15 1
rs13188991
GABRA6
1.000 0.040 5 161685998 synonymous variant G/A;C snv 0.19 0.18 1
rs1475196
HTR2A
1.000 0.040 13 46881488 intron variant A/C snv 1.4E-03 1
rs1618355
TRPM2
0.925 0.040 21 44406579 intron variant C/A;G snv 0.73; 1.7E-05 2
rs165599
ARVCF ; COMT
0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs17026688
GADL1
1.000 0.040 3 30845325 intron variant C/T snv 9.3E-03 2
rs17110566
TPH2
1.000 0.040 12 71972867 intron variant G/A snv 3.9E-02 1
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1935057
DAOA-AS1
1.000 0.040 13 105458997 upstream gene variant G/A snv 0.51 1
rs2197414
GABRA6
1.000 0.040 5 161681878 intron variant G/A;C snv 1
rs2217887
NRXN3
1.000 0.040 14 79417482 intron variant T/C snv 0.31 1
rs2230912
P2RX7 ; LOC105370032
0.752 0.280 12 121184393 missense variant A/G snv 0.13 0.12 16
rs2391191
DAOA-AS1 ; DAOA
0.807 0.080 13 105467097 missense variant G/A snv 0.40 0.32 7
rs2619522
DTNBP1
0.827 0.080 6 15653418 intron variant A/C snv 0.26 6
rs3757933
NRG1
1.000 0.040 8 32747325 intron variant G/A snv 0.23 1
rs3815762
GABRP
1.000 0.040 5 170788816 intron variant T/A snv 0.11 1
rs3916965 0.882 0.040 13 105451011 intergenic variant C/T snv 0.31 4
rs3916967
DAOA-AS1 ; DAOA
0.882 0.040 13 105464999 intron variant T/C snv 0.32 3
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249