Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1568523935
SLC25A42
0.776 0.240 19 19105656 stop gained C/G snv 20
rs1386494
TPH2
0.790 0.120 12 71958763 intron variant T/C;G snv 0.82 7
rs8192506
DBI
1.000 0.040 2 119372265 missense variant A/C;G snv 4.0E-06; 2.5E-02 2