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: rs1474868
rs1474868
1 1.000 0.040 1 11984107 intron variant C/T snv 0.53 0.010 1.000 1 2017 2017