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: rs10445371
rs10445371
MAPT
3 0.925 0.120 17 45988044 intron variant G/A snv 0.15 0.700 1.000 1 2012 2012
dbSNP: rs1529534
rs1529534
MAPT
2 1.000 0.080 17 45985774 intron variant A/G snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs17571718
rs17571718
MAPT
2 1.000 0.080 17 45955402 intron variant T/C snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs17571739
rs17571739
MAPT
3 0.925 0.120 17 45955549 intron variant T/C snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs17571781
rs17571781
MAPT
2 1.000 0.080 17 45956436 intron variant T/C;G snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs17571809
rs17571809
MAPT
3 0.925 0.120 17 45957493 intron variant A/G snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs17571857
rs17571857
MAPT
2 1.000 0.080 17 45958340 intron variant A/G snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs17572147
rs17572147
MAPT
2 1.000 0.080 17 45967619 intron variant A/G snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs17572169
rs17572169
MAPT
3 0.925 0.120 17 45968608 intron variant C/T snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs17572248
rs17572248
MAPT
2 1.000 0.080 17 45972501 intron variant A/G snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs17572361
rs17572361
MAPT
3 0.925 0.120 17 45974643 non coding transcript exon variant T/C snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs17572467
rs17572467
MAPT
2 1.000 0.080 17 45977022 non coding transcript exon variant T/C snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs17572495
rs17572495
MAPT
2 1.000 0.080 17 45977230 non coding transcript exon variant T/G snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs17572613
rs17572613
MAPT
2 1.000 0.080 17 45980638 intron variant A/G snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs17572627
rs17572627
MAPT
2 1.000 0.080 17 45981263 intron variant T/A snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs17572795
rs17572795
MAPT
2 1.000 0.080 17 45986027 intron variant G/A snv 0.15 0.700 1.000 1 2012 2012
dbSNP: rs17572823
rs17572823
MAPT
2 1.000 0.080 17 45986197 intron variant T/C snv 0.15 0.700 1.000 1 2012 2012
dbSNP: rs17572893
rs17572893
MAPT
2 1.000 0.080 17 45986842 intron variant G/A snv 0.15 0.700 1.000 1 2012 2012
dbSNP: rs17650771
rs17650771
MAPT
2 1.000 0.080 17 45958001 intron variant A/G snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs17650818
rs17650818
MAPT
2 1.000 0.080 17 45959421 intron variant T/C snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs17650842
rs17650842
MAPT
2 1.000 0.080 17 45960125 intron variant A/G snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs17650860
rs17650860
MAPT
2 1.000 0.080 17 45961642 intron variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs17650872
rs17650872
MAPT
2 1.000 0.080 17 45962150 intron variant G/T snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs17650901
rs17650901
MAPT
3 0.925 0.120 17 45962325 5 prime UTR variant A/G snv 0.14 0.14 0.700 1.000 1 2012 2012
dbSNP: rs17650973
rs17650973
MAPT
2 1.000 0.080 17 45966854 intron variant A/T snv 0.14 0.700 1.000 1 2012 2012