Source: ALL
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: rs3745567
rs3745567
C3
2 19 6690760 intron variant C/T snv 0.11 0.11 0.700 1.000 1 2012 2012
dbSNP: rs3753394
rs3753394
CFH
5 0.882 0.040 1 196651787 upstream gene variant C/T snv 0.22 0.700 1.000 1 2012 2012