Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs8019721
rs8019721
Entrez Id: 26037
Gene Symbol: SIPA1L1
SIPA1L1
CUI: C0429087
Disease:
Electrocardiogram: P-R interval 		A 0.700 GeneticVariation GWASCAT Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traits. 30679814 2019
dbSNP: rs75930676
rs75930676
Entrez Id: 26037
Gene Symbol: SIPA1L1
SIPA1L1
CUI: C4049938
Disease:
Physical Activity Measurement 		0.700 GeneticVariation GWASCAT Genome-wide association study of habitual physical activity in over 377,000 UK Biobank participants identifies multiple variants including CADM2 and APOE. 29899525 2018
dbSNP: rs11848785
rs11848785
Entrez Id: 26037
Gene Symbol: SIPA1L1
SIPA1L1
CUI: C0429097
Disease:
QRS complex feature 		0.700 GeneticVariation GWASCAT 52 Genetic Loci Influencing Myocardial Mass. 27659466 2016
dbSNP: rs12880291
rs12880291
Entrez Id: 26037
Gene Symbol: SIPA1L1
SIPA1L1
CUI: C0429097
Disease:
QRS complex feature 		0.700 GeneticVariation GWASCAT 52 Genetic Loci Influencing Myocardial Mass. 27659466 2016
dbSNP: rs17100926
rs17100926
Entrez Id: 26037
Gene Symbol: SIPA1L1
SIPA1L1
CUI: C0202236
Disease:
Triglycerides measurement 		A 0.700 GeneticVariation GWASCAT Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population. 23251661 2012
dbSNP: rs17100926
rs17100926
Entrez Id: 26037
Gene Symbol: SIPA1L1
SIPA1L1
CUI: C0392885
Disease:
High density lipoprotein measurement 		A 0.700 GeneticVariation GWASCAT Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population. 23251661 2012
dbSNP: rs17100926
rs17100926
Entrez Id: 26037
Gene Symbol: SIPA1L1
SIPA1L1
CUI: C0162701
Disease:
Polysomnography 		A 0.700 GeneticVariation GWASDB Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population. 23251661 2012
dbSNP: rs11848785
rs11848785
Entrez Id: 26037
Gene Symbol: SIPA1L1
SIPA1L1
CUI: C0018803
Disease:
Heart Function Tests 		G 0.700 GeneticVariation GWASDB Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. 21076409 2010