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: rs1799971
rs1799971
OPRM1
95 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 0.010 1.000 1 2014 2014
dbSNP: rs2511521
rs2511521
DRD2
1 1.000 0.080 11 113414577 intron variant G/A snv 0.59 0.010 1.000 1 2017 2017
dbSNP: rs625413
rs625413
TIRAP ; HP11014
1 1.000 0.080 11 126294454 3 prime UTR variant T/C snv 0.84 0.84 0.010 1.000 1 2017 2017