TAT, tyrosine aminotransferase, 6898

N. diseases: 230; N. variants: 28
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587776511
rs587776511
Entrez Id: 6898;100132529
Gene Symbol: TAT;TAT-AS1
TAT;TAT-AS1
CUI: C0268487
Disease:
Tyrosine Transaminase Deficiency Disease 		A 0.800 CausalMutation CLINVAR
dbSNP: rs587776511
rs587776511
Entrez Id: 6898;100132529
Gene Symbol: TAT;TAT-AS1
TAT;TAT-AS1
CUI: C0268487
Disease:
Tyrosine Transaminase Deficiency Disease 		0.800 GeneticVariation UNIPROT
dbSNP: rs113758103
rs113758103
Entrez Id: 6898;100132529
Gene Symbol: TAT;TAT-AS1
TAT;TAT-AS1
CUI: C0268487
Disease:
Tyrosine Transaminase Deficiency Disease 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs118203914
rs118203914
Entrez Id: 6898;100132529
Gene Symbol: TAT;TAT-AS1
TAT;TAT-AS1
CUI: C0268487
Disease:
Tyrosine Transaminase Deficiency Disease 		A 0.700 CausalMutation CLINVAR
dbSNP: rs118203915
rs118203915
Entrez Id: 6898;100132529
Gene Symbol: TAT;TAT-AS1
TAT;TAT-AS1
CUI: C0268487
Disease:
Tyrosine Transaminase Deficiency Disease 		C 0.700 CausalMutation CLINVAR
dbSNP: rs1426882225
rs1426882225
Entrez Id: 6898;100132529
Gene Symbol: TAT;TAT-AS1
TAT;TAT-AS1
CUI: C0268487
Disease:
Tyrosine Transaminase Deficiency Disease 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs1555537662
rs1555537662
Entrez Id: 6898;100132529
Gene Symbol: TAT;TAT-AS1
TAT;TAT-AS1
CUI: C0268487
Disease:
Tyrosine Transaminase Deficiency Disease 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs1555537673
rs1555537673
Entrez Id: 6898;100132529
Gene Symbol: TAT;TAT-AS1
TAT;TAT-AS1
CUI: C0268487
Disease:
Tyrosine Transaminase Deficiency Disease 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs1555537741
rs1555537741
Entrez Id: 6898;100132529
Gene Symbol: TAT;TAT-AS1
TAT;TAT-AS1
CUI: C0268487
Disease:
Tyrosine Transaminase Deficiency Disease 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs1555537814
rs1555537814
Entrez Id: 6898;100132529
Gene Symbol: TAT;TAT-AS1
TAT;TAT-AS1
CUI: C0268487
Disease:
Tyrosine Transaminase Deficiency Disease 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs1555537871
rs1555537871
Entrez Id: 6898;100132529
Gene Symbol: TAT;TAT-AS1
TAT;TAT-AS1
CUI: C0268487
Disease:
Tyrosine Transaminase Deficiency Disease 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs1555538138
rs1555538138
Entrez Id: 6898;100132529
Gene Symbol: TAT;TAT-AS1
TAT;TAT-AS1
CUI: C0268487
Disease:
Tyrosine Transaminase Deficiency Disease 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs587776512
rs587776512
Entrez Id: 6898;100132529
Gene Symbol: TAT;TAT-AS1
TAT;TAT-AS1
CUI: C0268487
Disease:
Tyrosine Transaminase Deficiency Disease 		C 0.700 CausalMutation CLINVAR
dbSNP: rs746077579
rs746077579
Entrez Id: 6898;100132529
Gene Symbol: TAT;TAT-AS1
TAT;TAT-AS1
CUI: C0268487
Disease:
Tyrosine Transaminase Deficiency Disease 		AG 0.700 GeneticVariation CLINVAR
dbSNP: rs748924248
rs748924248
Entrez Id: 6898;100132529
Gene Symbol: TAT;TAT-AS1
TAT;TAT-AS1
CUI: C0268487
Disease:
Tyrosine Transaminase Deficiency Disease 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs11075889
rs11075889
Entrez Id: 6898
Gene Symbol: TAT
TAT
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB Genome-wide association study identifies multiple loci influencing human serum metabolite levels. 22286219 2012
dbSNP: rs11862798
rs11862798
Entrez Id: 6898
Gene Symbol: TAT
TAT
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB Genome-wide association study identifies multiple loci influencing human serum metabolite levels. 22286219 2012
dbSNP: rs1477386
rs1477386
Entrez Id: 6898;100132529
Gene Symbol: TAT;TAT-AS1
TAT;TAT-AS1
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB Genome-wide association study identifies multiple loci influencing human serum metabolite levels. 22286219 2012
dbSNP: rs172650
rs172650
Entrez Id: 6898;100132529
Gene Symbol: TAT;TAT-AS1
TAT;TAT-AS1
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB Genome-wide association study identifies multiple loci influencing human serum metabolite levels. 22286219 2012
dbSNP: rs2432520
rs2432520
Entrez Id: 6898;100132529
Gene Symbol: TAT;TAT-AS1
TAT;TAT-AS1
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB Genome-wide association study identifies multiple loci influencing human serum metabolite levels. 22286219 2012
dbSNP: rs3829537
rs3829537
Entrez Id: 6898
Gene Symbol: TAT
TAT
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB Genome-wide association study identifies multiple loci influencing human serum metabolite levels. 22286219 2012
dbSNP: rs9930543
rs9930543
Entrez Id: 6898
Gene Symbol: TAT
TAT
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB Genome-wide association study identifies multiple loci influencing human serum metabolite levels. 22286219 2012
dbSNP: rs1555538156
rs1555538156
Entrez Id: 6898;100132529
Gene Symbol: TAT;TAT-AS1
TAT;TAT-AS1
CUI: C0268487
Disease:
Tyrosine Transaminase Deficiency Disease 		CA 0.700 GeneticVariation CLINVAR Herpetiform keratitis and palmoplantar hyperkeratosis: warning signs for Richner-Hanhart syndrome. 27832414 2017
dbSNP: rs118203914
rs118203914
Entrez Id: 6898;100132529
Gene Symbol: TAT;TAT-AS1
TAT;TAT-AS1
CUI: C0268487
Disease:
Tyrosine Transaminase Deficiency Disease 		A 0.700 GeneticVariation CLINVAR Novel and recurrent tyrosine aminotransferase gene mutations in tyrosinemia type II. 9544843 1998
dbSNP: rs761817519
rs761817519
Entrez Id: 6898;100132529
Gene Symbol: TAT;TAT-AS1
TAT;TAT-AS1
CUI: C0268487
Disease:
Tyrosine Transaminase Deficiency Disease 		A 0.700 GeneticVariation CLINVAR Novel and recurrent tyrosine aminotransferase gene mutations in tyrosinemia type II. 9544843 1998