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: rs2179593
rs2179593
11 0.790 0.080 20 44031646 intron variant C/A snv 0.71 0.700 1.000 1 2019 2019
dbSNP: rs6031311
rs6031311
10 0.776 0.080 20 44037835 intron variant C/T snv 0.73 0.700 1.000 1 2019 2019