Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs183716
rs183716
Entrez Id: 79042;79143
Gene Symbol: TSEN34;MBOAT7
TSEN34;MBOAT7
CUI: C0162701
Disease:
Polysomnography 		0.700 GeneticVariation GWASDB Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population. 23251661 2012
dbSNP: rs40357
rs40357
Entrez Id: 79042;79143
Gene Symbol: TSEN34;MBOAT7
TSEN34;MBOAT7
CUI: C0162701
Disease:
Polysomnography 		0.700 GeneticVariation GWASDB Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population. 23251661 2012
dbSNP: rs7595
rs7595
Entrez Id: 79042
Gene Symbol: TSEN34
TSEN34
CUI: C0162701
Disease:
Polysomnography 		G 0.700 GeneticVariation GWASDB Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population. 23251661 2012
dbSNP: rs7595
rs7595
Entrez Id: 79042
Gene Symbol: TSEN34
TSEN34
CUI: C0005890
Disease:
Body Height 		G 0.700 GeneticVariation GWASCAT Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population. 23251661 2012
dbSNP: rs113994150
rs113994150
Entrez Id: 79042;79143
Gene Symbol: TSEN34;MBOAT7
TSEN34;MBOAT7
CUI: C2676465
Disease:
Pontocerebellar Hypoplasia Type 2C 		T 0.700 CausalMutation CLINVAR
dbSNP: rs113994150
rs113994150
Entrez Id: 79042;79143
Gene Symbol: TSEN34;MBOAT7
TSEN34;MBOAT7
CUI: C1848526
Disease:
Pontocerebellar Hypoplasia Type 2A 		T 0.700 CausalMutation CLINVAR
dbSNP: rs886041058
rs886041058
Entrez Id: 79042;79143
Gene Symbol: TSEN34;MBOAT7
TSEN34;MBOAT7
CUI: C4310673
Disease:
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 57 		T 0.700 CausalMutation CLINVAR