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: rs2332036
rs2332036
1 3 121995544 intron variant C/T snv 0.38 0.700 1.000 1 2019 2019
dbSNP: rs9816720
rs9816720
1 3 121995837 intron variant G/A snv 0.41 0.700 1.000 1 2018 2018