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: rs1898671
rs1898671
5 0.851 0.160 5 111072304 intron variant C/T snv 0.25 0.710 1.000 2 2011 2019