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: 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 2007 2007
dbSNP: rs63750349
rs63750349
MAPT
5 0.851 0.200 17 45996638 missense variant C/G;T snv 4.0E-06 0.010 1.000 1 2007 2007