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: rs17012216
rs17012216
1 4 86968285 intron variant G/T snv 0.17 0.700 1.000 1 2018 2018
dbSNP: rs6840258
rs6840258
2 4 87052516 intron variant C/T snv 0.21 0.700 1.000 1 2016 2016