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: rs1012053
rs1012053
1 1.000 0.040 13 42079301 intron variant C/A snv 0.85 0.800 1.000 1 2008 2008