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: rs2811710
rs2811710
1 1.000 0.160 9 21991924 intron variant C/T snv 0.47 0.700 1.000 1 2016 2016