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: rs63750424
rs63750424
MAPT
30 0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 0.700 0
dbSNP: rs63750756
rs63750756
MAPT
23 0.716 0.200 17 46010324 missense variant T/G snv 2.6E-05 0.700 0
dbSNP: rs63751273
rs63751273
MAPT
42 0.645 0.280 17 46010389 missense variant C/T snv 0.700 0
dbSNP: rs63751392
rs63751392
MAPT
2 0.925 0.120 17 46010371 inframe deletion ATA/- delins 0.700 0
dbSNP: rs62063857
rs62063857
MAPT ; STH
3 0.882 0.120 17 45999299 missense variant A/G snv 0.14 0.15 0.010 1.000 1 2015 2015