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: rs373359894
rs373359894
C5
1 1.000 9 120997684 missense variant G/A;T snv 1.6E-05; 4.0E-06 0.700 0
dbSNP: rs56040400
rs56040400
C5
1 1.000 9 120997683 missense variant C/T snv 3.3E-04 1.0E-04 0.700 0