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: rs1038822
rs1038822
1 1.000 0.120 2 43511034 intron variant T/A;C snv 0.700 1.000 1 2011 2011