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: rs80358247
rs80358247
3 0.882 0.080 1 154191993 missense variant A/C snv 4.0E-06 0.710 1.000 1 2002 2002
dbSNP: rs121964852
rs121964852
4 0.851 0.080 1 154172971 missense variant C/T snv 0.010 1.000 1 2008 2008
dbSNP: rs199474714
rs199474714
4 0.925 0.080 1 154173113 missense variant C/T snv 0.010 1.000 1 2010 2010