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 0.700 1.000 1 2017 2017
dbSNP: rs202073531
rs202073531
ACP4 ; LOC105372439
1 1.000 19 50791683 missense variant C/T snv 1.3E-04 1.1E-04 0.700 1.000 1 2016 2016
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 0.700 1.000 1 2017 2017
dbSNP: rs763573828
rs763573828
ACP4 ; LOC105372439
1 1.000 19 50793751 missense variant C/T snv 8.0E-06 0.700 1.000 1 2016 2016
dbSNP: rs779823931
rs779823931
ACP4 ; LOC105372439
1 1.000 19 50791749 missense variant G/A snv 8.1E-06 7.0E-06 0.700 1.000 1 2016 2016
dbSNP: rs1057519277
rs1057519277
ACP4 ; LOC105372439
1 1.000 19 50790783 missense variant C/G;T snv 6.6E-06; 2.0E-05 0.700 0
dbSNP: rs767907487
rs767907487
ACP4 ; LOC105372439
1 1.000 19 50791734 missense variant G/C snv 2.4E-05 0.700 0