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: rs4680
rs4680
155 0.484 0.821 22 19963748 missense variant G/A snp 0.46 0.45 0.020 1.000 2 2018 2018
dbSNP: rs1799971
rs1799971
57 0.611 0.500 6 154039662 missense variant A/G snp 0.19 0.12 0.010 1.000 1 2013 2013
dbSNP: rs1800497
rs1800497
36 0.662 0.250 11 113400106 missense variant G/A snp 0.26 0.26 0.010 1.000 1 2010 2010
dbSNP: rs1843809
rs1843809
3 0.923 0.036 12 71954918 intron variant G/T snp 0.77 0.010 1.000 1 2010 2010
dbSNP: rs2402959
rs2402959
1 7 129765967 intergenic variant A/G snp 0.27 0.010 1.000 1 2014 2014
dbSNP: rs2519152
rs2519152
DBH
2 1.000 0.036 9 133644512 intron variant T/C snp 0.40 0.010 1.000 1 2013 2013
dbSNP: rs373611092
rs373611092
3 1.000 0.036 22 19962794 missense variant A/G snp 8.4E-05 1.3E-04 0.010 1.000 1 2013 2013
dbSNP: rs6565113
rs6565113
3 0.923 0.036 16 83074041 intron variant G/C,T snp 0.61 0.010 1.000 1 2010 2010
dbSNP: rs6965643
rs6965643
1 7 129767724 regulatory region variant A/G snp 0.28 0.010 1.000 1 2014 2014
dbSNP: rs7794745
rs7794745
6 0.923 0.036 7 146792514 intron variant A/T snp 0.49 0.010 1.000 1 2010 2010