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: rs751563679
rs751563679
1 1.000 0.120 5 87389444 missense variant C/T snv 4.0E-06 0.010 1.000 1 2003 2003
dbSNP: rs899638423
rs899638423
1 1.000 0.120 5 87268495 missense variant C/T snv 7.1E-06 0.010 1.000 1 2009 2009