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: rs1050976
rs1050976
4 0.851 0.280 6 408079 3 prime UTR variant C/T snv 0.37 0.700 1.000 1 2018 2018
dbSNP: rs12203592
rs12203592
38 0.649 0.320 6 396321 intron variant C/T snv 0.10 0.010 1.000 1 2016 2016
dbSNP: rs872071
rs872071
13 0.742 0.360 6 411064 3 prime UTR variant A/G;T snv 0.010 1.000 1 2016 2016