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: rs58190593
rs58190593
2 19 19153129 intron variant C/T snv 0.16 0.700 1.000 2 2018 2018
dbSNP: rs75746498
rs75746498
2 19 19149877 intron variant G/A;C;T snv 0.700 1.000 1 2018 2018