Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs369100678
rs369100678
Entrez Id: 54832
Gene Symbol: VPS13C
VPS13C
CUI: C4225186
Disease:
PARKINSON DISEASE 23, AUTOSOMAL RECESSIVE EARLY-ONSET 		0.800 GeneticVariation UNIPROT Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy. 26942284 2016
dbSNP: rs17271305
rs17271305
Entrez Id: 54832
Gene Symbol: VPS13C
VPS13C
CUI: C0017741
Disease:
Glucose tolerance test 		G 0.800 GeneticVariation GWASDB Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge. 20081857 2010
dbSNP: rs17271305
rs17271305
Entrez Id: 54832
Gene Symbol: VPS13C
VPS13C
CUI: C0017741
Disease:
Glucose tolerance test 		G 0.800 GeneticVariation GWASCAT Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge. 20081857 2010
dbSNP: rs369100678
rs369100678
Entrez Id: 54832
Gene Symbol: VPS13C
VPS13C
CUI: C4225186
Disease:
PARKINSON DISEASE 23, AUTOSOMAL RECESSIVE EARLY-ONSET 		G 0.800 CausalMutation CLINVAR
dbSNP: rs933807
rs933807
Entrez Id: 54832
Gene Symbol: VPS13C
VPS13C
CUI: C0424678
Disease:
Lean body mass 		0.700 GeneticVariation GWASCAT Genomics of body fat percentage may contribute to sex bias in anorexia nervosa. 30593698 2019
dbSNP: rs17271340
rs17271340
Entrez Id: 54832
Gene Symbol: VPS13C
VPS13C
CUI: C0017741
Disease:
Glucose tolerance test 		0.700 GeneticVariation GWASCAT Fast and Accurate Genome-Wide Association Test of Multiple Quantitative Traits. 29743933 2018
dbSNP: rs17271340
rs17271340
Entrez Id: 54832
Gene Symbol: VPS13C
VPS13C
CUI: C0428568
Disease:
Fasting blood glucose measurement 		0.700 GeneticVariation GWASCAT Fast and Accurate Genome-Wide Association Test of Multiple Quantitative Traits. 29743933 2018
dbSNP: rs2042608
rs2042608
Entrez Id: 54832
Gene Symbol: VPS13C
VPS13C
CUI: C0017741
Disease:
Glucose tolerance test 		0.700 GeneticVariation GWASCAT Fast and Accurate Genome-Wide Association Test of Multiple Quantitative Traits. 29743933 2018
dbSNP: rs2042608
rs2042608
Entrez Id: 54832
Gene Symbol: VPS13C
VPS13C
CUI: C0428568
Disease:
Fasting blood glucose measurement 		0.700 GeneticVariation GWASCAT Fast and Accurate Genome-Wide Association Test of Multiple Quantitative Traits. 29743933 2018
dbSNP: rs72749754
rs72749754
Entrez Id: 54832
Gene Symbol: VPS13C
VPS13C
CUI: C1305855
Disease:
Body mass index 		C 0.700 GeneticVariation GWASCAT Genome-wide association study identifies 112 new loci for body mass index in the Japanese population. 28892062 2017
dbSNP: rs148713408
rs148713408
Entrez Id: 54832
Gene Symbol: VPS13C
VPS13C
CUI: C0425782
Disease:
Breast size 		0.700 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965 2016
dbSNP: rs369100678
rs369100678
Entrez Id: 54832
Gene Symbol: VPS13C
VPS13C
CUI: C0030567
Disease:
Parkinson Disease 		G 0.700 CausalMutation CLINVAR Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy. 26942284 2016
dbSNP: rs869312809
rs869312809
Entrez Id: 54832
Gene Symbol: VPS13C
VPS13C
CUI: C0030567
Disease:
Parkinson Disease 		C 0.700 CausalMutation CLINVAR Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy. 26942284 2016
dbSNP: rs869312810
rs869312810
Entrez Id: 54832
Gene Symbol: VPS13C
VPS13C
CUI: C0030567
Disease:
Parkinson Disease 		A 0.700 CausalMutation CLINVAR Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy. 26942284 2016
dbSNP: rs869312811
rs869312811
Entrez Id: 54832
Gene Symbol: VPS13C
VPS13C
CUI: C0030567
Disease:
Parkinson Disease 		T 0.700 CausalMutation CLINVAR Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy. 26942284 2016
dbSNP: rs879253853
rs879253853
Entrez Id: 54832
Gene Symbol: VPS13C
VPS13C
CUI: C0030567
Disease:
Parkinson Disease 		TTCTG 0.700 CausalMutation CLINVAR Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy. 26942284 2016
dbSNP: rs869312809
rs869312809
Entrez Id: 54832
Gene Symbol: VPS13C
VPS13C
CUI: C4225186
Disease:
PARKINSON DISEASE 23, AUTOSOMAL RECESSIVE EARLY-ONSET 		C 0.700 CausalMutation CLINVAR
dbSNP: rs869312810
rs869312810
Entrez Id: 54832
Gene Symbol: VPS13C
VPS13C
CUI: C4225186
Disease:
PARKINSON DISEASE 23, AUTOSOMAL RECESSIVE EARLY-ONSET 		A 0.700 CausalMutation CLINVAR
dbSNP: rs869312811
rs869312811
Entrez Id: 54832
Gene Symbol: VPS13C
VPS13C
CUI: C4225186
Disease:
PARKINSON DISEASE 23, AUTOSOMAL RECESSIVE EARLY-ONSET 		T 0.700 CausalMutation CLINVAR
dbSNP: rs869320761
rs869320761
Entrez Id: 54832
Gene Symbol: VPS13C
VPS13C
CUI: C4225186
Disease:
PARKINSON DISEASE 23, AUTOSOMAL RECESSIVE EARLY-ONSET 		CTCTG 0.700 CausalMutation CLINVAR