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: rs4327090
rs4327090
1 17 45825175 intron variant A/G snv 0.12 0.700 1.000 1 2018 2018
dbSNP: rs62057107
rs62057107
1 17 45818666 intron variant C/G;T snv 0.700 1.000 1 2018 2018