MAPT, microtubule associated protein tau, 4137

N. diseases: 469; N. variants: 292
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2435207
rs2435207
1.000 0.040 17 45981562 intron variant G/A snv 0.30
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.010 < 0.001 1 2009 2009
dbSNP: rs3785883
rs3785883
0.925 0.080 17 45977067 non coding transcript exon variant A/G snv 0.81
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.010 < 0.001 1 2009 2009
dbSNP: rs7521
rs7521
0.925 0.080 17 46028029 3 prime UTR variant A/C;G snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.010 1.000 1 2009 2009
dbSNP: rs1433515721
rs1433515721
1.000 0.040 17 45996618 missense variant A/G snv 4.0E-06 7.0E-06
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.010 1.000 1 2010 2010
dbSNP: rs1461089499
rs1461089499
1.000 0.040 17 46023990 missense variant C/T snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.010 1.000 1 2010 2010
dbSNP: rs17563965
rs17563965
1.000 0.040 17 45913553 intron variant A/G snv 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.010 1.000 1 2010 2010
dbSNP: rs17649641
rs17649641
0.925 0.120 17 45920006 intron variant T/C snv 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.010 1.000 1 2010 2010
dbSNP: rs17564983
rs17564983
1.000 0.040 17 45934459 intron variant A/C snv 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs1864325
rs1864325
0.882 0.160 17 45900461 intron variant C/T snv 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs1991556
rs1991556
1.000 0.040 17 46006036 intron variant G/A snv 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs2435200
rs2435200
0.925 0.080 17 45994485 intron variant G/A snv 0.40
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs3785880
rs3785880
1.000 0.040 17 45916010 intron variant T/G snv 0.40
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs4792891
rs4792891
1.000 0.040 17 45896132 non coding transcript exon variant T/G snv 0.30
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs767057
rs767057
0.925 0.120 17 45921456 intron variant A/G snv 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs1052553
rs1052553
0.827 0.200 17 45996523 synonymous variant A/G snv 0.14 0.15
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.730 0.750 4 2010 2012
dbSNP: rs1800547
rs1800547
0.925 0.120 17 45974480 non coding transcript exon variant A/G snv 0.15 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.720 1.000 4 2008 2012
dbSNP: rs1981997
rs1981997
1.000 0.040 17 45979401 non coding transcript exon variant G/A snv 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.700 1.000 3 2009 2012
dbSNP: rs10445337
rs10445337
0.925 0.120 17 45990034 missense variant T/C snv 0.15 0.15
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs10445338
rs10445338
1.000 0.040 17 45990316 intron variant G/A snv 0.15
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs1052551
rs1052551
1.000 0.040 17 45991558 synonymous variant G/A;T snv 0.14; 8.0E-05
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs1052587
rs1052587
0.925 0.120 17 46025238 3 prime UTR variant T/C snv 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs1078268
rs1078268
0.925 0.120 17 45998535 intron variant A/G snv 0.15
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs17573175
rs17573175
1.000 0.040 17 45993723 intron variant C/G;T snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs17574228
rs17574228
0.925 0.120 17 46027143 3 prime UTR variant T/C snv 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs17650901
rs17650901
0.925 0.120 17 45962325 5 prime UTR variant A/G snv 0.14 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.700 1.000 1 2012 2012