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: rs11574944
rs11574944
1 1.000 0.200 16 30498669 intron variant C/T snv 0.25 0.010 1.000 1 2014 2014