SBNO1, strawberry notch homolog 1, 55206

N. diseases: 39; N. variants: 9
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4759375
rs4759375
Entrez Id: 55206
Gene Symbol: SBNO1
SBNO1
CUI: C0392885
Disease:
High density lipoprotein measurement
T 0.800 GeneticVariation GWASCAT Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids. 30926973 2019
dbSNP: rs4759375
rs4759375
Entrez Id: 55206
Gene Symbol: SBNO1
SBNO1
CUI: C0392885
Disease:
High density lipoprotein measurement
T 0.800 GeneticVariation GWASCAT Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program. 30275531 2018
dbSNP: rs4759375
rs4759375
Entrez Id: 55206
Gene Symbol: SBNO1
SBNO1
CUI: C0392885
Disease:
High density lipoprotein measurement
C 0.800 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422 2018
dbSNP: rs4759375
rs4759375
Entrez Id: 55206
Gene Symbol: SBNO1
SBNO1
CUI: C0392885
Disease:
High density lipoprotein measurement
T 0.800 GeneticVariation GWASDB Discovery and refinement of loci associated with lipid levels. 24097068 2013
dbSNP: rs4759375
rs4759375
Entrez Id: 55206
Gene Symbol: SBNO1
SBNO1
CUI: C0392885
Disease:
High density lipoprotein measurement
T 0.800 GeneticVariation GWASCAT Discovery and refinement of loci associated with lipid levels. 24097068 2013
dbSNP: rs4759375
rs4759375
Entrez Id: 55206
Gene Symbol: SBNO1
SBNO1
CUI: C0392885
Disease:
High density lipoprotein measurement
T 0.800 GeneticVariation GWASCAT Biological, clinical and population relevance of 95 loci for blood lipids. 20686565 2010
dbSNP: rs4759375
rs4759375
Entrez Id: 55206
Gene Symbol: SBNO1
SBNO1
CUI: C0392885
Disease:
High density lipoprotein measurement
T 0.800 GeneticVariation GWASDB Biological, clinical and population relevance of 95 loci for blood lipids. 20686565 2010
dbSNP: rs11057270
rs11057270
Entrez Id: 55206
Gene Symbol: SBNO1
SBNO1
CUI: C1861172
Disease:
Venous Thromboembolism
0.700 GeneticVariation GWASCAT Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism. 31420334 2019
dbSNP: rs56116847
rs56116847
Entrez Id: 55206
Gene Symbol: SBNO1
SBNO1
CUI: C0409959
Disease:
Osteoarthritis, Knee
A 0.700 GeneticVariation GWASCAT Identification of new therapeutic targets for osteoarthritis through genome-wide analyses of UK Biobank data. 30664745 2019
dbSNP: rs7298909
rs7298909
Entrez Id: 55206
Gene Symbol: SBNO1
SBNO1
CUI: C0001948
Disease:
Alcohol consumption
T 0.700 GeneticVariation GWASCAT Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions. 30698716 2019
dbSNP: rs7298909
rs7298909
Entrez Id: 55206
Gene Symbol: SBNO1
SBNO1
CUI: C0392885
Disease:
High density lipoprotein measurement
T 0.700 GeneticVariation GWASCAT Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions. 30698716 2019
dbSNP: rs77866843
rs77866843
Entrez Id: 55206
Gene Symbol: SBNO1
SBNO1
CUI: C0023508
Disease:
White Blood Cell Count procedure
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1060105
rs1060105
Entrez Id: 55206
Gene Symbol: SBNO1
SBNO1
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
C 0.700 GeneticVariation GWASCAT Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes. 29632382 2018
dbSNP: rs1060105
rs1060105
Entrez Id: 55206
Gene Symbol: SBNO1
SBNO1
CUI: C0409959
Disease:
Osteoarthritis, Knee
C 0.700 GeneticVariation GWASCAT Meta-analysis of Icelandic and UK data sets identifies missense variants in SMO, IL11, COL11A1 and 13 more new loci associated with osteoarthritis. 30374069 2018
dbSNP: rs4759375
rs4759375
Entrez Id: 55206
Gene Symbol: SBNO1
SBNO1
CUI: C1445957
Disease:
Serum total cholesterol measurement
C 0.700 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422 2018
dbSNP: rs10773003
rs10773003
Entrez Id: 55206
Gene Symbol: SBNO1
SBNO1
CUI: C0392885
Disease:
High density lipoprotein measurement
A 0.700 GeneticVariation GWASCAT Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels. 28334899 2017
dbSNP: rs7980687
rs7980687
Entrez Id: 55206
Gene Symbol: SBNO1
SBNO1
CUI: C0428883
Disease:
Diastolic blood pressure
G 0.700 GeneticVariation GWASCAT Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation. 27841878 2017
dbSNP: rs1060105
rs1060105
Entrez Id: 55206
Gene Symbol: SBNO1
SBNO1
CUI: C0428883
Disease:
Diastolic blood pressure
T 0.700 GeneticVariation GWASCAT Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension. 27618447 2016
dbSNP: rs7980687
rs7980687
Entrez Id: 55206
Gene Symbol: SBNO1
SBNO1
CUI: C0005890
Disease:
Body Height
A 0.700 GeneticVariation GWASCAT Defining the role of common variation in the genomic and biological architecture of adult human height. 25282103 2014
dbSNP: rs4759375
rs4759375
Entrez Id: 55206
Gene Symbol: SBNO1
SBNO1
CUI: C0428472
Disease:
Serum HDL cholesterol measurement
T 0.700 GeneticVariation GWASDB Discovery and refinement of loci associated with lipid levels. 24097068 2013
dbSNP: rs11830103
rs11830103
Entrez Id: 55206
Gene Symbol: SBNO1
SBNO1
CUI: C0005890
Disease:
Body Height
A 0.700 GeneticVariation GWASCAT Hundreds of variants clustered in genomic loci and biological pathways affect human height. 20881960 2010
dbSNP: rs11830103
rs11830103
Entrez Id: 55206
Gene Symbol: SBNO1
SBNO1
CUI: C0489786
Disease:
Height
A 0.700 GeneticVariation GWASDB Hundreds of variants clustered in genomic loci and biological pathways affect human height. 20881960 2010
dbSNP: rs4759375
rs4759375
Entrez Id: 55206
Gene Symbol: SBNO1
SBNO1
CUI: C0428472
Disease:
Serum HDL cholesterol measurement
T 0.700 GeneticVariation GWASDB Biological, clinical and population relevance of 95 loci for blood lipids. 20686565 2010