Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12705932
rs12705932
Entrez Id: 5506
Gene Symbol: PPP1R3A
PPP1R3A
CUI: C0202117
Disease:
Low density lipoprotein cholesterol measurement
G 0.700 GeneticVariation GWASCAT Analysis of pleiotropic genetic effects on cognitive impairment, systemic inflammation, and plasma lipids in the Health and Retirement Study. 31201950 2019
dbSNP: rs71571192
rs71571192
Entrez Id: 5506
Gene Symbol: PPP1R3A
PPP1R3A
CUI: C1445957
Disease:
Serum total cholesterol measurement
T 0.700 GeneticVariation GWASCAT Analysis of pleiotropic genetic effects on cognitive impairment, systemic inflammation, and plasma lipids in the Health and Retirement Study. 31201950 2019
dbSNP: rs1799999
rs1799999
Entrez Id: 5506
Gene Symbol: PPP1R3A
PPP1R3A
CUI: C1852091
Disease:
INSULIN RESISTANCE, SUSCEPTIBILITY TO
A 0.700 SusceptibilityMutation CLINVAR
dbSNP: rs35449651
rs35449651
Entrez Id: 5506
Gene Symbol: PPP1R3A
PPP1R3A
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.700 GeneticVariation UNIPROT
dbSNP: rs1799999
rs1799999
Entrez Id: 5506
Gene Symbol: PPP1R3A
PPP1R3A
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.040 GeneticVariation BEFREE For the first time, rs1799999 in PPP1R3A was associated with risk of T2D in Mayan Mexican individuals (OR = 1.625, P = 0.014). 29948331 2018
dbSNP: rs1799999
rs1799999
Entrez Id: 5506
Gene Symbol: PPP1R3A
PPP1R3A
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.040 GeneticVariation BEFREE The analyses revealed that INS (rs689) polymorphism conferred risk towards T2D susceptibility in all the three ethnic groups whereas INSR (rs1799816) polymorphism conferred risk towards T2D in Brahmins only and PP1G.G (rs1799999) polymorphism indicated T2D risk in Jat Sikhs only. 26251103 2016
dbSNP: rs1799999
rs1799999
Entrez Id: 5506
Gene Symbol: PPP1R3A
PPP1R3A
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.040 GeneticVariation BEFREE In conclusion, we found no evidence in Swedish men that the PP1ARE or the Asp905Tyr variants over a 20-year period predict the development of IGT or type 2 diabetes, but the PP1ARE polymorphism could have a higher penetrance in other populations. 10868947 2000
dbSNP: rs1799999
rs1799999
Entrez Id: 5506
Gene Symbol: PPP1R3A
PPP1R3A
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.040 GeneticVariation BEFREE These data suggest that the Asp905Tyr polymorphism of the PPP1R3 gene is not associated with NIDDM or high BMI, both of which are known to be insulin-resistant states, in the Japanese population. 9653600 1998
dbSNP: rs1799999
rs1799999
Entrez Id: 5506
Gene Symbol: PPP1R3A
PPP1R3A
CUI: C0494463
Disease:
Alzheimer Disease, Late Onset
0.010 GeneticVariation BEFREE Additionally, in the dominant genetic model a marginally significant association in genotype frequencies between the Asp905Tyr PPP1R3 polymorphism and AD was observed (genotypes: OR 1.85, 95% CI 1.03 to 3.30, p = 0.04; alleles: OR 1.68, 95% CI 0.98 to 2.88, p = 0.06). 12185156 2002
dbSNP: rs1799999
rs1799999
Entrez Id: 5506
Gene Symbol: PPP1R3A
PPP1R3A
CUI: C0271650
Disease:
Impaired glucose tolerance
0.010 GeneticVariation BEFREE In conclusion, we found no evidence in Swedish men that the PP1ARE or the Asp905Tyr variants over a 20-year period predict the development of IGT or type 2 diabetes, but the PP1ARE polymorphism could have a higher penetrance in other populations. 10868947 2000