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: rs1127354
rs1127354
26 0.667 0.400 20 3213196 missense variant C/A;G snv 7.5E-02 0.020 1.000 2 2013 2019
dbSNP: rs137852314
rs137852314
4 0.851 0.120 X 154534495 missense variant C/T snv 4.4E-05 5.7E-05 0.010 1.000 1 2017 2017
dbSNP: rs1799793
rs1799793
72 0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 0.010 1.000 1 2019 2019
dbSNP: rs2072671
rs2072671
CDA
16 0.752 0.280 1 20589208 missense variant A/C snv 0.28 0.25 0.010 < 0.001 1 2015 2015
dbSNP: rs267607201
rs267607201
7 0.807 0.120 19 12885001 missense variant C/T snv 0.010 1.000 1 2018 2018
dbSNP: rs751661633
rs751661633
6 0.851 0.120 22 38984136 missense variant C/A snv 4.1E-06 0.010 < 0.001 1 2015 2015