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: rs2789845
rs2789845
5 1.000 9 133934793 intron variant C/T snv 0.80 0.700 1.000 1 2019 2019