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: rs141138948
rs141138948
9 0.807 0.120 9 37783993 missense variant T/C;G snv 4.1E-04 0.030 1.000 3 2013 2018
dbSNP: rs387907196
rs387907196
12 0.807 0.080 9 37784953 missense variant C/G snv 2.0E-05 0.020 1.000 2 2013 2018
dbSNP: rs374550999
rs374550999
2 0.925 0.080 9 37784807 missense variant C/A;G snv 1.5E-04 0.010 1.000 1 2013 2013