PLIN2, perilipin 2, 123

N. diseases: 100; N. variants: 3
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs111791351
rs111791351
Entrez Id: 123
Gene Symbol: PLIN2
PLIN2
CUI: C0871470
Disease:
Systolic Pressure
T 0.700 GeneticVariation GWASCAT Trans-ethnic association study of blood pressure determinants in over 750,000 individuals. 30578418 2019
dbSNP: rs35568725
rs35568725
Entrez Id: 123
Gene Symbol: PLIN2
PLIN2
CUI: C0020459
Disease:
Hyperinsulinism
0.010 GeneticVariation BEFREE The perilipin 2 (PLIN2) gene Ser251Pro missense mutation is associated with reduced insulin secretion and increased insulin sensitivity in Italian obese subjects. 26443937 2016
dbSNP: rs35568725
rs35568725
Entrez Id: 123
Gene Symbol: PLIN2
PLIN2
CUI: C0028754
Disease:
Obesity
0.010 GeneticVariation BEFREE The aim of this study was to evaluate the effect of the Ser251Pro mutation of PLIN2 gene in a cohort with a higher predisposition to obesity-associated metabolic alterations, such as insulin resistance, decreased insulin-secretion, hyperglycaemia, and dyslipidaemia. 26443937 2016
dbSNP: rs35568725
rs35568725
Entrez Id: 123
Gene Symbol: PLIN2
PLIN2
CUI: C0242339
Disease:
Dyslipidemias
0.010 GeneticVariation BEFREE The aim of this study was to evaluate the effect of the Ser251Pro mutation of PLIN2 gene in a cohort with a higher predisposition to obesity-associated metabolic alterations, such as insulin resistance, decreased insulin-secretion, hyperglycaemia, and dyslipidaemia. 26443937 2016
dbSNP: rs768322837
rs768322837
Entrez Id: 123
Gene Symbol: PLIN2
PLIN2
CUI: C0035334
Disease:
Retinitis Pigmentosa
0.010 GeneticVariation BEFREE We found three different unreported mutations 689delT, 857del17, corresponding to two macular dystrophy families and G208D in a retinitis pigmentosa (RP) family giving us a proportion of about 20% of RDS mutations in autosomal dominant Spanish macular dystrophies and 3% in ADRP. 10627133 1998