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: rs9397080
rs9397080
2 1.000 0.040 6 152059380 intron variant C/T snv 0.22 0.010 1.000 1 2012 2012