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: rs11951673
rs11951673
3 5 96525308 non coding transcript exon variant C/T snv 0.39 0.700 1.000 1 2012 2012
dbSNP: rs6882366
rs6882366
2 5 96528989 intron variant C/T snv 0.39 0.700 1.000 1 2012 2012