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: rs370717845
rs370717845
HGSNAT
33 0.763 0.320 8 43161462 missense variant G/A snv 0.700 0
dbSNP: rs1003921
rs1003921
KCNC1
1 1.000 0.040 11 17778789 intron variant G/A;C snv 0.010 1.000 1 2014 2014
dbSNP: rs1998220
rs1998220
OPRM1 ; IPCEF1
1 1.000 0.040 6 154185294 intron variant A/G snv 0.63 0.010 1.000 1 2014 2014
dbSNP: rs4938056
rs4938056
HTR3B
2 0.925 0.080 11 113915817 intron variant C/T snv 0.51 0.010 1.000 1 2014 2014
dbSNP: rs9534511
rs9534511
HTR2A
1 1.000 0.040 13 46894445 intron variant T/C snv 0.54 0.010 1.000 1 2014 2014