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: rs7903146
rs7903146
93 0.554 0.680 10 112998590 intron variant C/G;T snv 0.030 1.000 3 2014 2018
dbSNP: rs290487
rs290487
10 0.776 0.280 10 113149972 intron variant C/T snv 0.16 0.010 1.000 1 2018 2018