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: rs4478858
rs4478858
3 1.000 0.080 1 31411078 intron variant T/C snv 0.48 0.800 1.000 1 2013 2013