Gene: MAPT ×
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: rs63750869
rs63750869
MAPT
6 0.827 0.160 17 46018707 missense variant G/A snv 2.4E-05 5.6E-05 0.020 1.000 2 2007 2011
dbSNP: rs267604921
rs267604921
MAPT
3 0.925 0.160 17 45993953 missense variant C/A;G;T snv 6.3E-05; 2.5E-04; 5.3E-06 0.010 1.000 1 2016 2016
dbSNP: rs533610448
rs533610448
MAPT
3 0.882 0.240 17 45983334 missense variant A/T snv 9.8E-05 6.3E-05 0.010 1.000 1 2016 2016
dbSNP: rs63750756
rs63750756
MAPT
23 0.716 0.200 17 46010324 missense variant T/G snv 2.6E-05 0.010 1.000 1 2016 2016
dbSNP: rs63751273
rs63751273
MAPT
42 0.645 0.280 17 46010389 missense variant C/T snv 0.010 1.000 1 2016 2016
dbSNP: rs762046989
rs762046989
MAPT
5 0.851 0.200 17 45971867 missense variant C/G snv 8.0E-06 0.010 1.000 1 2016 2016
dbSNP: rs762104961
rs762104961
MAPT
3 0.882 0.200 17 46024014 missense variant C/T snv 4.0E-06 0.010 1.000 1 2016 2016