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: rs17563986
rs17563986
MAPT
4 1.000 0.040 17 45913906 intron variant A/G snv 0.14 0.700 1.000 4 2009 2014
dbSNP: rs1981997
rs1981997
MAPT
3 1.000 0.040 17 45979401 non coding transcript exon variant G/A snv 0.14 0.700 1.000 3 2009 2012
dbSNP: rs242562
rs242562
MAPT
2 1.000 0.040 17 45949373 intron variant G/A snv 0.35 0.020 0.500 2 2009 2014
dbSNP: rs10445338
rs10445338
MAPT
2 1.000 0.040 17 45990316 intron variant G/A snv 0.15 0.700 1.000 1 2012 2012
dbSNP: rs1052551
rs1052551
MAPT
1 1.000 0.040 17 45991558 synonymous variant G/A;T snv 0.14; 8.0E-05 0.700 1.000 1 2012 2012
dbSNP: rs1433515721
rs1433515721
MAPT
1 1.000 0.040 17 45996618 missense variant A/G snv 4.0E-06 7.0E-06 0.010 1.000 1 2010 2010
dbSNP: rs1461089499
rs1461089499
MAPT
1 1.000 0.040 17 46023990 missense variant C/T snv 0.010 1.000 1 2010 2010
dbSNP: rs17563965
rs17563965
MAPT
2 1.000 0.040 17 45913553 intron variant A/G snv 0.14 0.010 1.000 1 2010 2010
dbSNP: rs17564983
rs17564983
MAPT ; LOC105371800
2 1.000 0.040 17 45934459 intron variant A/C snv 0.14 0.700 1.000 1 2011 2011
dbSNP: rs17573175
rs17573175
MAPT
2 1.000 0.040 17 45993723 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs17691610
rs17691610
MAPT ; MAPT-AS1
2 1.000 0.040 17 45893296 intron variant G/T snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs17770343
rs17770343
MAPT ; MAPT-AS1
2 1.000 0.040 17 45892788 intron variant T/C snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs1991556
rs1991556
MAPT
4 1.000 0.040 17 46006036 intron variant G/A snv 0.14 0.700 1.000 1 2011 2011
dbSNP: rs2435207
rs2435207
MAPT
2 1.000 0.040 17 45981562 intron variant G/A snv 0.30 0.010 < 0.001 1 2009 2009
dbSNP: rs3785880
rs3785880
MAPT
2 1.000 0.040 17 45916010 intron variant T/G snv 0.40 0.010 1.000 1 2011 2011
dbSNP: rs4792891
rs4792891
MAPT ; MAPT-AS1 ; MAPT-IT1
1 1.000 0.040 17 45896132 non coding transcript exon variant T/G snv 0.30 0.700 1.000 1 2011 2011
dbSNP: rs769851761
rs769851761
MAPT
1 1.000 0.040 17 46024136 missense variant G/A snv 8.0E-06 0.010 1.000 1 2016 2016
dbSNP: rs9468
rs9468
MAPT
6 0.882 0.080 17 46024197 3 prime UTR variant T/C snv 0.15 0.14 0.030 1.000 3 2012 2019
dbSNP: rs2435200
rs2435200
MAPT
5 0.925 0.080 17 45994485 intron variant G/A snv 0.40 0.010 1.000 1 2011 2011
dbSNP: rs3785883
rs3785883
MAPT
2 0.925 0.080 17 45977067 non coding transcript exon variant A/G snv 0.81 0.010 < 0.001 1 2009 2009
dbSNP: rs7521
rs7521
MAPT ; KANSL1
3 0.925 0.080 17 46028029 3 prime UTR variant A/C;G snv 0.010 1.000 1 2009 2009
dbSNP: rs1800547
rs1800547
MAPT
3 0.925 0.120 17 45974480 non coding transcript exon variant A/G snv 0.15 0.14 0.720 1.000 4 2008 2012
dbSNP: rs62063857
rs62063857
MAPT ; STH
3 0.882 0.120 17 45999299 missense variant A/G snv 0.14 0.15 0.730 0.750 4 2010 2017
dbSNP: rs10445337
rs10445337
MAPT
3 0.925 0.120 17 45990034 missense variant T/C snv 0.15 0.15 0.700 1.000 1 2012 2012
dbSNP: rs1052587
rs1052587
MAPT
3 0.925 0.120 17 46025238 3 prime UTR variant T/C snv 0.14 0.700 1.000 1 2012 2012