Gene: MAPT ×
Source: GWASCAT ×
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: rs2471738
rs2471738
MAPT ; STH
1 0.882 0.160 17 45998697 intron variant C/T snv 0.18 0.700 1.000 2 2018 2018
dbSNP: rs17563986
rs17563986
MAPT
1 1.000 0.040 17 45913906 intron variant A/G snv 0.14 0.700 1.000 1 2017 2017
dbSNP: rs242559
rs242559
MAPT
1 1.000 0.080 17 45948522 intron variant C/A snv 0.71 0.700 1.000 1 2018 2018
dbSNP: rs28646281
rs28646281
MAPT
1 17 45900480 intron variant T/C;G snv 0.700 1.000 1 2018 2018
dbSNP: rs713522
rs713522
MAPT
1 17 45987897 intron variant T/C snv 0.44 0.700 1.000 1 2018 2018
dbSNP: rs754593
rs754593
MAPT
3 1.000 0.040 17 45977330 non coding transcript exon variant G/A snv 0.52 0.700 1.000 1 2018 2018
dbSNP: rs8065165
rs8065165
MAPT ; MAPT-AS1
1 17 45892951 intron variant C/T snv 0.12 0.700 1.000 1 2018 2018
dbSNP: rs8067056
rs8067056
MAPT
4 0.925 0.080 17 46006582 intron variant T/C;G snv 0.30 0.700 1.000 1 2018 2018