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: rs1101999
rs1101999
1 1.000 0.080 1 158962765 intron variant C/T snv 0.92 0.800 1.000 1 2011 2011