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: rs1991556
rs1991556
MAPT
4 1.000 0.040 17 46006036 intron variant G/A snv 0.14 0.700 1.000 1 2018 2018
dbSNP: rs62061734
rs62061734
MAPT
2 1.000 0.080 17 45941122 intron variant T/A;C snv 0.700 1.000 1 2019 2019