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: rs211105
rs211105
4 1.000 11 18033757 intron variant T/G snv 0.19 0.010 1.000 1 2018 2018