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: rs2287019
rs2287019
7 1.000 0.080 19 45698914 intron variant C/T snv 0.17 0.16 0.700 1.000 2 2010 2013