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: rs5016282
rs5016282
1 1.000 0.040 11 89008492 intron variant A/G snv 0.800 1.000 1 2011 2011