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: rs754093
rs754093
1 18 79486406 missense variant T/A;G snv 1.2E-05; 0.42 0.010 1.000 1 2011 2011
dbSNP: rs864321650
rs864321650
3 5 173234902 missense variant G/A;C snv 0.010 1.000 1 2009 2009