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: rs3765598
rs3765598
1 1.000 0.080 1 113851841 intron variant C/T snv 0.15 0.020 1.000 2 2013 2016