MAPT, microtubule associated protein tau, 4137

N. diseases: 469; N. variants: 292
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs63751438
rs63751438
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
CUI: C0338451
Disease:
Frontotemporal dementia
T 0.900 CausalMutation CLINVAR
dbSNP: rs63750570
rs63750570
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
CUI: C0338451
Disease:
Frontotemporal dementia
A 0.850 CausalMutation CLINVAR
dbSNP: rs63750349
rs63750349
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
CUI: C0338451
Disease:
Frontotemporal dementia
G 0.830 CausalMutation CLINVAR
dbSNP: rs63751165
rs63751165
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
CUI: C0338451
Disease:
Frontotemporal dementia
A 0.830 CausalMutation CLINVAR
dbSNP: rs63751165
rs63751165
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
CUI: C0338451
Disease:
Frontotemporal dementia
0.830 GeneticVariation UNIPROT
dbSNP: rs63750129
rs63750129
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
CUI: C0236642
Disease:
Pick Disease of the Brain
C 0.820 CausalMutation CLINVAR
dbSNP: rs63750376
rs63750376
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
CUI: C0338451
Disease:
Frontotemporal dementia
T 0.820 CausalMutation CLINVAR
dbSNP: rs63750512
rs63750512
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
CUI: C0236642
Disease:
Pick Disease of the Brain
A 0.820 CausalMutation CLINVAR
dbSNP: rs63750635
rs63750635
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
CUI: C0236642
Disease:
Pick Disease of the Brain
T 0.810 CausalMutation CLINVAR
dbSNP: rs63750711
rs63750711
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
CUI: C0338451
Disease:
Frontotemporal dementia
T 0.810 CausalMutation CLINVAR
dbSNP: rs63751264
rs63751264
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
CUI: C0236642
Disease:
Pick Disease of the Brain
T 0.810 CausalMutation CLINVAR
dbSNP: rs63751264
rs63751264
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
CUI: C0236642
Disease:
Pick Disease of the Brain
0.810 GeneticVariation UNIPROT
dbSNP: rs63750092
rs63750092
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
CUI: C0338451
Disease:
Frontotemporal dementia
T 0.800 CausalMutation CLINVAR
dbSNP: rs63750424
rs63750424
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
CUI: C0338451
Disease:
Frontotemporal dementia
T 0.800 CausalMutation CLINVAR
dbSNP: rs63750756
rs63750756
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
CUI: C0236642
Disease:
Pick Disease of the Brain
G 0.800 CausalMutation CLINVAR
dbSNP: rs63750959
rs63750959
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
CUI: C4551863
Disease:
Supranuclear Palsy, Progressive, 1
0.800 GeneticVariation UNIPROT
dbSNP: rs63750959
rs63750959
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
CUI: C4551863
Disease:
Supranuclear Palsy, Progressive, 1
T 0.800 CausalMutation CLINVAR
dbSNP: rs63751273
rs63751273
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
CUI: C0236642
Disease:
Pick Disease of the Brain
T 0.800 CausalMutation CLINVAR
dbSNP: rs63751391
rs63751391
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
CUI: C4551863
Disease:
Supranuclear Palsy, Progressive, 1
0.800 GeneticVariation UNIPROT
dbSNP: rs63751391
rs63751391
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
CUI: C4551863
Disease:
Supranuclear Palsy, Progressive, 1
T 0.800 CausalMutation CLINVAR
dbSNP: rs63750424
rs63750424
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
CUI: C0236642
Disease:
Pick Disease of the Brain
T 0.760 CausalMutation CLINVAR
dbSNP: rs1568327531
rs1568327531
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
CUI: C0338451
Disease:
Frontotemporal dementia
A 0.700 CausalMutation CLINVAR
dbSNP: rs1568339821
rs1568339821
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
CUI: C0338451
Disease:
Frontotemporal dementia
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1568339995
rs1568339995
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
CUI: C0002395
Disease:
Alzheimer's Disease
T 0.700 GeneticVariation CLINVAR
dbSNP: rs63750308
rs63750308
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
CUI: C0338451
Disease:
Frontotemporal dementia
G 0.700 CausalMutation CLINVAR