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: rs4859584
rs4859584
1 1.000 0.040 4 76021984 intron variant G/C snv 0.61 0.61 0.010 1.000 1 2015 2015