PTS, 6-pyruvoyltetrahydropterin synthase, 5805

N. diseases: 89; N. variants: 40
Disease: Hyperphenylalaninaemia ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894275
rs104894275
Entrez Id: 5805
Gene Symbol: PTS
PTS
CUI: C0751435
Disease:
Hyperphenylalaninaemia 		0.010 GeneticVariation BEFREE By analysis of 38 PTPS mutant alleles from 19 unrelated Chinese PTPS-deficient HPA families, the allele frequency of these mutations in Chinese PTPS-deficient HPA were determined to be approximately 5.3% (R25G), 34.2% (N52S), 7.9% (V56M), 2.6% (V70D), 36.8% (P87S), 7.9% (D96N), and 2.6% (T106M), respectively. 9450907 1998
dbSNP: rs104894276
rs104894276
Entrez Id: 5805
Gene Symbol: PTS
PTS
CUI: C0751435
Disease:
Hyperphenylalaninaemia 		0.010 GeneticVariation BEFREE By analysis of 38 PTPS mutant alleles from 19 unrelated Chinese PTPS-deficient HPA families, the allele frequency of these mutations in Chinese PTPS-deficient HPA were determined to be approximately 5.3% (R25G), 34.2% (N52S), 7.9% (V56M), 2.6% (V70D), 36.8% (P87S), 7.9% (D96N), and 2.6% (T106M), respectively. 9450907 1998
dbSNP: rs104894277
rs104894277
Entrez Id: 5805
Gene Symbol: PTS
PTS
CUI: C0751435
Disease:
Hyperphenylalaninaemia 		0.010 GeneticVariation BEFREE By analysis of 38 PTPS mutant alleles from 19 unrelated Chinese PTPS-deficient HPA families, the allele frequency of these mutations in Chinese PTPS-deficient HPA were determined to be approximately 5.3% (R25G), 34.2% (N52S), 7.9% (V56M), 2.6% (V70D), 36.8% (P87S), 7.9% (D96N), and 2.6% (T106M), respectively. 9450907 1998
dbSNP: rs104894280
rs104894280
Entrez Id: 5805
Gene Symbol: PTS
PTS
CUI: C0751435
Disease:
Hyperphenylalaninaemia 		0.010 GeneticVariation BEFREE By analysis of 38 PTPS mutant alleles from 19 unrelated Chinese PTPS-deficient HPA families, the allele frequency of these mutations in Chinese PTPS-deficient HPA were determined to be approximately 5.3% (R25G), 34.2% (N52S), 7.9% (V56M), 2.6% (V70D), 36.8% (P87S), 7.9% (D96N), and 2.6% (T106M), respectively. 9450907 1998
dbSNP: rs1167104933
rs1167104933
Entrez Id: 5805
Gene Symbol: PTS
PTS
CUI: C0751435
Disease:
Hyperphenylalaninaemia 		0.010 GeneticVariation BEFREE By analysis of 38 PTPS mutant alleles from 19 unrelated Chinese PTPS-deficient HPA families, the allele frequency of these mutations in Chinese PTPS-deficient HPA were determined to be approximately 5.3% (R25G), 34.2% (N52S), 7.9% (V56M), 2.6% (V70D), 36.8% (P87S), 7.9% (D96N), and 2.6% (T106M), respectively. 9450907 1998
dbSNP: rs200712908
rs200712908
Entrez Id: 5805
Gene Symbol: PTS
PTS
CUI: C0751435
Disease:
Hyperphenylalaninaemia 		0.010 GeneticVariation BEFREE By analysis of 38 PTPS mutant alleles from 19 unrelated Chinese PTPS-deficient HPA families, the allele frequency of these mutations in Chinese PTPS-deficient HPA were determined to be approximately 5.3% (R25G), 34.2% (N52S), 7.9% (V56M), 2.6% (V70D), 36.8% (P87S), 7.9% (D96N), and 2.6% (T106M), respectively. 9450907 1998