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: rs2040862
rs2040862
1 1.000 0.080 5 138084300 intron variant C/T snv 0.13 0.13 0.800 1.000 2 2012 2018