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: rs1085307111
rs1085307111
ACP4 ; LOC105372439
3 0.882 0.080 19 50793784 missense variant C/T snv 0.010 1.000 1 2017 2017
dbSNP: rs546603773
rs546603773
ACP4 ; LOC105372439
3 0.882 0.080 19 50791780 missense variant C/A;G;T snv 8.3E-06; 8.3E-06; 5.4E-05 0.010 1.000 1 2017 2017