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: rs1057516159
rs1057516159
6 0.827 0.240 3 138946383 missense variant T/C snv 0.010 1.000 1 2011 2011
dbSNP: rs121908359
rs121908359
4 0.851 0.240 3 138946163 missense variant C/T snv 4.5E-05 7.0E-06 0.010 1.000 1 2009 2009