Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10042486
rs10042486 		4 0.882 0.040 5 63965502 intron variant C/T snv 0.58 0.010 1.000 1 2013 2013
dbSNP: rs1801028
rs1801028
DRD2
24 0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02 0.010 1.000 1 2004 2004
dbSNP: rs2023239
rs2023239
CNR1
20 0.724 0.160 6 88150763 intron variant T/C snv 0.21 0.010 1.000 1 2015 2015
dbSNP: rs6675281
rs6675281
DISC2 ; DISC1 ; TSNAX-DISC1 ; LOC105373170
7 0.827 0.080 1 231818355 missense variant C/T snv 0.11 0.14 0.010 1.000 1 2008 2008
dbSNP: rs7139958
rs7139958
DAOA ; DAOA-AS1
2 1.000 0.040 13 105484383 intron variant T/A snv 0.32 0.010 1.000 1 2013 2013