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: rs5743867
rs5743867
3 0.882 0.120 11 1307121 intron variant G/A;C snv 0.010 1.000 1 2018 2018
dbSNP: rs5743899
rs5743899
6 0.807 0.160 11 1302334 intron variant C/T snv 0.71 0.010 1.000 1 2018 2018