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: rs1416122398
rs1416122398
1 1.000 0.080 9 21974791 missense variant C/A;G snv 4.3E-06 0.020 0.500 2 2008 2013
dbSNP: rs3731201
rs3731201
2 1.000 0.080 9 21988897 intron variant C/T snv 0.86 0.010 1.000 1 2010 2010