MEIS1, Meis homeobox 1, 4211

N. diseases: 104; N. variants: 19
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2300478
rs2300478
Entrez Id: 4211
Gene Symbol: MEIS1
MEIS1
CUI: C0035258
Disease:
Restless Legs Syndrome 		0.820 GeneticVariation BEFREE The most significant SNP of MEIS1, rs2300478, increased the risk of RLS by 1.42-fold in the overall cohort ( p = 0.0047). 26643377 2016
dbSNP: rs2300478
rs2300478
Entrez Id: 4211
Gene Symbol: MEIS1
MEIS1
CUI: C0035258
Disease:
Restless Legs Syndrome 		G 0.820 GeneticVariation GWASCAT Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1. 21779176 2011
dbSNP: rs2300478
rs2300478
Entrez Id: 4211
Gene Symbol: MEIS1
MEIS1
CUI: C0035258
Disease:
Restless Legs Syndrome 		G 0.820 GeneticVariation GWASDB Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1. 21779176 2011
dbSNP: rs2300478
rs2300478
Entrez Id: 4211
Gene Symbol: MEIS1
MEIS1
CUI: C0035258
Disease:
Restless Legs Syndrome 		0.820 GeneticVariation BEFREE Case-control association studies showed significant association between all three variants and RLS (P=0.0001/OR=1.65, P=0.0021/OR=1.59, and P=0.0011/OR=1.55 for rs2300478, rs9357271, and rs1026732, respectively). 21925394 2011
dbSNP: rs2300478
rs2300478
Entrez Id: 4211
Gene Symbol: MEIS1
MEIS1
CUI: C0035258
Disease:
Restless Legs Syndrome 		G 0.820 GeneticVariation GWASCAT Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions. 17637780 2007
dbSNP: rs2300478
rs2300478
Entrez Id: 4211
Gene Symbol: MEIS1
MEIS1
CUI: C0035258
Disease:
Restless Legs Syndrome 		G 0.820 GeneticVariation GWASDB Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions. 17637780 2007
dbSNP: rs10865355
rs10865355
Entrez Id: 4211
Gene Symbol: MEIS1
MEIS1
CUI: C0429087
Disease:
Electrocardiogram: P-R interval 		0.800 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584 2019
dbSNP: rs11897119
rs11897119
Entrez Id: 4211
Gene Symbol: MEIS1
MEIS1
CUI: C0429087
Disease:
Electrocardiogram: P-R interval 		0.800 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584 2019
dbSNP: rs3891585
rs3891585
Entrez Id: 4211
Gene Symbol: MEIS1
MEIS1
CUI: C0429087
Disease:
Electrocardiogram: P-R interval 		0.800 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584 2019
dbSNP: rs3891585
rs3891585
Entrez Id: 4211
Gene Symbol: MEIS1
MEIS1
CUI: C0429087
Disease:
Electrocardiogram: P-R interval 		A 0.800 GeneticVariation GWASDB Novel loci associated with PR interval in a genome-wide association study of 10 African American cohorts. 23139255 2012
dbSNP: rs3891585
rs3891585
Entrez Id: 4211
Gene Symbol: MEIS1
MEIS1
CUI: C0429087
Disease:
Electrocardiogram: P-R interval 		A 0.800 GeneticVariation GWASCAT Novel loci associated with PR interval in a genome-wide association study of 10 African American cohorts. 23139255 2012
dbSNP: rs10865355
rs10865355
Entrez Id: 4211
Gene Symbol: MEIS1
MEIS1
CUI: C0429087
Disease:
Electrocardiogram: P-R interval 		A 0.800 GeneticVariation GWASCAT Genome-wide association studies of the PR interval in African Americans. 21347284 2011
dbSNP: rs10865355
rs10865355
Entrez Id: 4211
Gene Symbol: MEIS1
MEIS1
CUI: C0429087
Disease:
Electrocardiogram: P-R interval 		0.800 GeneticVariation GWASDB Genome-wide association studies of the PR interval in African Americans. 21347284 2011
dbSNP: rs3891585
rs3891585
Entrez Id: 4211
Gene Symbol: MEIS1
MEIS1
CUI: C0429087
Disease:
Electrocardiogram: P-R interval 		0.800 GeneticVariation GWASDB Genome-wide association studies of the PR interval in African Americans. 21347284 2011
dbSNP: rs11897119
rs11897119
Entrez Id: 4211
Gene Symbol: MEIS1
MEIS1
CUI: C0429087
Disease:
Electrocardiogram: P-R interval 		C 0.800 GeneticVariation GWASCAT Genome-wide association study of PR interval. 20062060 2010
dbSNP: rs11897119
rs11897119
Entrez Id: 4211
Gene Symbol: MEIS1
MEIS1
CUI: C0429087
Disease:
Electrocardiogram: P-R interval 		C 0.800 GeneticVariation GWASDB Genome-wide association study of PR interval. 20062060 2010
dbSNP: rs11897119
rs11897119
Entrez Id: 4211
Gene Symbol: MEIS1
MEIS1
CUI: C0205682
Disease:
Waist-Hip Ratio 		T 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry. 30239722 2019
dbSNP: rs13033745
rs13033745
Entrez Id: 4211;730198
Gene Symbol: MEIS1;MEIS1-AS3
MEIS1;MEIS1-AS3
CUI: C0023508
Disease:
White Blood Cell Count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs13033745
rs13033745
Entrez Id: 4211;730198
Gene Symbol: MEIS1;MEIS1-AS3
MEIS1;MEIS1-AS3
CUI: C0200638
Disease:
Eosinophil count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2300481
rs2300481
Entrez Id: 4211
Gene Symbol: MEIS1
MEIS1
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: rs6724747
rs6724747
Entrez Id: 4211
Gene Symbol: MEIS1
MEIS1
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: rs9798015
rs9798015
Entrez Id: 4211
Gene Symbol: MEIS1
MEIS1
CUI: C0205682
Disease:
Waist-Hip Ratio 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs113851554
rs113851554
Entrez Id: 4211
Gene Symbol: MEIS1
MEIS1
CUI: C0424574
Disease:
Duration of sleep 		G 0.700 GeneticVariation GWASCAT GWAS identifies 14 loci for device-measured physical activity and sleep duration. 30531941 2018
dbSNP: rs113851554
rs113851554
Entrez Id: 4211
Gene Symbol: MEIS1
MEIS1
CUI: C0008810
Disease:
Circadian Rhythms 		0.700 GeneticVariation GWASCAT Genome-Wide Association Study of Circadian Rhythmicity in 71,500 UK Biobank Participants and Polygenic Association with Mood Instability. 30120083 2018
dbSNP: rs1519104
rs1519104
Entrez Id: 4211
Gene Symbol: MEIS1
MEIS1
CUI: C0202236
Disease:
Triglycerides measurement 		A 0.700 GeneticVariation GWASCAT Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program. 30275531 2018