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: rs338598
rs338598
1 1.000 0.120 19 41195623 intron variant C/A;G;T snv 0.700 1.000 1 2019 2019