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: rs708272
rs708272
24 0.708 0.440 16 56962376 intron variant G/A snv 0.42 0.38 0.030 1.000 3 2016 2019
dbSNP: rs5882
rs5882
35 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 0.020 1.000 2 2018 2019
dbSNP: rs1800775
rs1800775
18 0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 0.010 1.000 1 2019 2019
dbSNP: rs4783961
rs4783961
7 0.851 0.320 16 56960982 upstream gene variant G/A snv 0.48 0.47 0.010 1.000 1 2019 2019