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: rs9620953
rs9620953
1 1.000 0.080 22 30150256 intron variant C/T snv 0.20 0.700 1.000 1 2011 2011