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: rs62398709
rs62398709
1 5 152675675 intron variant A/T snv 0.34 0.700 1.000 1 2018 2018
dbSNP: rs6895232
rs6895232
1 5 152659861 intron variant T/A;C snv 0.700 1.000 1 2018 2018