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: rs11220082
rs11220082
1 1.000 0.040 11 125454069 intron variant C/T snv 0.46 0.800 1.000 1 2011 2012