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: rs121909065
rs121909065
1 1.000 0.080 5 71719903 missense variant G/C snv 1.3E-04 6.3E-05 0.720 1.000 2 2006 2006
dbSNP: rs78242624
rs78242624
1 1.000 0.080 5 71719917 missense variant G/A;C snv 4.0E-06; 1.0E-03 0.010 1.000 1 2000 2000