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: rs12607903
rs12607903
1 18 3817134 intron variant C/T snv 0.64 0.700 1.000 2 2014 2019
dbSNP: rs35212912
rs35212912
1 18 3816054 intron variant -/C ins 0.700 1.000 1 2016 2016