Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267607261
rs267607261
Entrez Id: 4358
Gene Symbol: MPV17
MPV17
CUI: C0234146
Disease:
Absent reflex 		T 0.700 CausalMutation CLINVAR
dbSNP: rs368900406
rs368900406
Entrez Id: 4358
Gene Symbol: MPV17
MPV17
CUI: C0234146
Disease:
Absent reflex 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs267607261
rs267607261
Entrez Id: 4358
Gene Symbol: MPV17
MPV17
CUI: C0003079
Disease:
Anisocoria 		T 0.700 CausalMutation CLINVAR
dbSNP: rs368900406
rs368900406
Entrez Id: 4358
Gene Symbol: MPV17
MPV17
CUI: C0003079
Disease:
Anisocoria 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs4665965
rs4665965
Entrez Id: 4358
Gene Symbol: MPV17
MPV17
CUI: C0003868
Disease:
Arthritis, Gouty 		0.700 GeneticVariation GWASDB Genome-wide association analyses identify 18 new loci associated with serum urate concentrations. 23263486 2013
dbSNP: rs267607261
rs267607261
Entrez Id: 4358
Gene Symbol: MPV17
MPV17
CUI: C0005745
Disease:
Blepharoptosis 		T 0.700 CausalMutation CLINVAR
dbSNP: rs368900406
rs368900406
Entrez Id: 4358
Gene Symbol: MPV17
MPV17
CUI: C0005745
Disease:
Blepharoptosis 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs267607261
rs267607261
Entrez Id: 4358
Gene Symbol: MPV17
MPV17
CUI: C0856863
Disease:
Broad-based gait 		T 0.700 CausalMutation CLINVAR
dbSNP: rs368900406
rs368900406
Entrez Id: 4358
Gene Symbol: MPV17
MPV17
CUI: C0856863
Disease:
Broad-based gait 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs267607261
rs267607261
Entrez Id: 4358
Gene Symbol: MPV17
MPV17
CUI: C1295585
Disease:
Decreased vibratory sense 		T 0.700 CausalMutation CLINVAR
dbSNP: rs368900406
rs368900406
Entrez Id: 4358
Gene Symbol: MPV17
MPV17
CUI: C1295585
Disease:
Decreased vibratory sense 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs267607261
rs267607261
Entrez Id: 4358
Gene Symbol: MPV17
MPV17
CUI: C0241237
Disease:
Difficulty standing 		T 0.700 CausalMutation CLINVAR
dbSNP: rs368900406
rs368900406
Entrez Id: 4358
Gene Symbol: MPV17
MPV17
CUI: C0241237
Disease:
Difficulty standing 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs267607261
rs267607261
Entrez Id: 4358
Gene Symbol: MPV17
MPV17
CUI: C0311394
Disease:
Difficulty walking 		T 0.700 CausalMutation CLINVAR
dbSNP: rs368900406
rs368900406
Entrez Id: 4358
Gene Symbol: MPV17
MPV17
CUI: C0311394
Disease:
Difficulty walking 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs267607261
rs267607261
Entrez Id: 4358
Gene Symbol: MPV17
MPV17
CUI: C1836451
Disease:
Distal lower limb amyotrophy 		T 0.700 CausalMutation CLINVAR
dbSNP: rs368900406
rs368900406
Entrez Id: 4358
Gene Symbol: MPV17
MPV17
CUI: C1836451
Disease:
Distal lower limb amyotrophy 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs267607261
rs267607261
Entrez Id: 4358
Gene Symbol: MPV17
MPV17
CUI: C1836450
Disease:
Distal lower limb muscle weakness 		T 0.700 CausalMutation CLINVAR
dbSNP: rs368900406
rs368900406
Entrez Id: 4358
Gene Symbol: MPV17
MPV17
CUI: C1836450
Disease:
Distal lower limb muscle weakness 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs267607261
rs267607261
Entrez Id: 4358
Gene Symbol: MPV17
MPV17
CUI: C3150620
Disease:
Distal upper limb muscle weakness 		T 0.700 CausalMutation CLINVAR
dbSNP: rs368900406
rs368900406
Entrez Id: 4358
Gene Symbol: MPV17
MPV17
CUI: C3150620
Disease:
Distal upper limb muscle weakness 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs4665965
rs4665965
Entrez Id: 4358
Gene Symbol: MPV17
MPV17
CUI: C0428568
Disease:
Fasting blood glucose measurement 		0.700 GeneticVariation GWASDB Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways. 22885924 2012
dbSNP: rs4665965
rs4665965
Entrez Id: 4358
Gene Symbol: MPV17
MPV17
CUI: C1261430
Disease:
Fasting blood sugar result 		0.700 GeneticVariation GWASDB Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways. 22885924 2012
dbSNP: rs267607261
rs267607261
Entrez Id: 4358
Gene Symbol: MPV17
MPV17
CUI: C1836150
Disease:
Gait imbalance 		T 0.700 CausalMutation CLINVAR
dbSNP: rs368900406
rs368900406
Entrez Id: 4358
Gene Symbol: MPV17
MPV17
CUI: C1836150
Disease:
Gait imbalance 		C 0.700 GeneticVariation CLINVAR