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: rs121918584
rs121918584
RBP4 ; FFAR4
2 0.925 0.040 10 93600739 missense variant A/T snv 0.010 1.000 1 2005 2005
dbSNP: rs121918585
rs121918585
RBP4 ; FFAR4
2 0.925 0.040 10 93600470 missense variant C/T snv 0.010 1.000 1 2005 2005