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: rs748954737
rs748954737
CRP
3 0.882 0.040 1 159713734 missense variant C/T snv 4.0E-06 0.010 1.000 1 2006 2006
dbSNP: rs77832441
rs77832441
CRP
3 0.882 0.040 1 159714024 missense variant G/A snv 1.4E-03 1.6E-03 0.010 < 0.001 1 2015 2015
dbSNP: rs3091244
rs3091244
CRP
17 0.724 0.280 1 159714875 upstream gene variant G/A;T snv 0.010 1.000 1 2006 2006