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: rs1035071612
rs1035071612
LDLR ; MIR6886
9 0.763 0.240 19 11113361 missense variant C/A;T snv 4.0E-06 0.010 1.000 1 2002 2002
dbSNP: rs1182182524
rs1182182524
MAPT
3 0.882 0.120 17 45983724 missense variant T/G snv 1.4E-05 0.010 1.000 1 2008 2008
dbSNP: rs1294621609
rs1294621609
MAPT
1 1.000 17 45996462 missense variant G/C;T snv 4.1E-06 0.010 1.000 1 2013 2013
dbSNP: rs63750082
rs63750082
PSEN1
13 0.732 0.120 14 73192712 missense variant G/C;T snv 8.0E-06 0.010 1.000 1 2013 2013
dbSNP: rs63750418
rs63750418
PSEN1
3 0.882 0.120 14 73186877 missense variant T/C snv 0.010 1.000 1 2013 2013
dbSNP: rs63751273
rs63751273
MAPT
42 0.645 0.280 17 46010389 missense variant C/T snv 0.010 1.000 1 2013 2013
dbSNP: rs669
rs669
A2M ; KLRG1
7 0.851 0.080 12 9079672 missense variant T/C snv 0.31 0.33 0.010 1.000 1 2002 2002