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: rs10083558
rs10083558
1 15 90659273 intron variant C/A snv 0.30 0.700 1.000 1 2019 2019
dbSNP: rs2010672
rs2010672
2 15 90658042 intron variant G/C;T snv 0.700 1.000 1 2016 2016