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: rs72928364
rs72928364
2 1.000 0.080 3 100894935 intron variant C/T snv 0.39 0.700 1.000 1 2017 2017