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: rs63750959
rs63750959
MAPT
5 0.827 0.200 17 45962351 missense variant G/A;T snv 6.0E-05 0.800 0
dbSNP: rs63751391
rs63751391
MAPT
3 0.882 0.120 17 46010395 missense variant G/T snv 0.800 0
dbSNP: rs63750424
rs63750424
MAPT
30 0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 0.700 0
dbSNP: rs63750425
rs63750425
MAPT
1 1.000 0.120 17 46018675 missense variant C/T snv 7.0E-06 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