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: rs165656
rs165656
COMT
5 0.925 0.200 22 19961340 intron variant G/A;C;T snv 0.010 1.000 1 2019 2019
dbSNP: rs1923886
rs1923886
HTR2A
1 13 46849156 intron variant C/T snv 0.64 0.010 1.000 1 2019 2019
dbSNP: rs1985242
rs1985242
HTR3A
1 11 113977551 5 prime UTR variant A/C;T snv 2.6E-05; 0.63 0.010 1.000 1 2019 2019
dbSNP: rs2070762
rs2070762
TH
5 0.925 0.080 11 2165105 intron variant A/G snv 0.43 0.010 1.000 1 2019 2019
dbSNP: rs4633
rs4633
COMT ; MIR4761
25 0.695 0.400 22 19962712 synonymous variant C/T snv 0.46 0.45 0.010 1.000 1 2019 2019
dbSNP: rs7330636
rs7330636
HTR2A
1 13 46849457 intron variant C/T snv 0.42 0.010 1.000 1 2019 2019