NCOR1, nuclear receptor corepressor 1, 9611

N. diseases: 94; N. variants: 9
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1075901
rs1075901
Entrez Id: 9611;54902
Gene Symbol: NCOR1;TTC19
NCOR1;TTC19
CUI: C1305855
Disease:
Body mass index
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: rs1075901
rs1075901
Entrez Id: 9611;54902
Gene Symbol: NCOR1;TTC19
NCOR1;TTC19
CUI: C1305855
Disease:
Body mass index
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs34351630
rs34351630
Entrez Id: 9611
Gene Symbol: NCOR1
NCOR1
CUI: C0016529
Disease:
Forced expiratory volume function
T 0.700 GeneticVariation GWASCAT New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. 30804560 2019
dbSNP: rs34351630
rs34351630
Entrez Id: 9611
Gene Symbol: NCOR1
NCOR1
CUI: C0042834
Disease:
Vital capacity
T 0.700 GeneticVariation GWASCAT New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. 30804560 2019
dbSNP: rs11078333
rs11078333
Entrez Id: 9611
Gene Symbol: NCOR1
NCOR1
CUI: C0202231
Disease:
Thyroxine measurement
A 0.700 GeneticVariation GWASCAT Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation. 30367059 2018
dbSNP: rs178810
rs178810
Entrez Id: 9611
Gene Symbol: NCOR1
NCOR1
CUI: C0201657
Disease:
C-reactive protein measurement
T 0.700 GeneticVariation GWASCAT Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders. 30388399 2018
dbSNP: rs4792721
rs4792721
Entrez Id: 9611
Gene Symbol: NCOR1
NCOR1
CUI: C0016529
Disease:
Forced expiratory volume function
A 0.700 GeneticVariation GWASCAT Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation. 26635082 2015
dbSNP: rs7218945
rs7218945
Entrez Id: 9611
Gene Symbol: NCOR1
NCOR1
CUI: C0202117
Disease:
Low density lipoprotein cholesterol measurement
0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs7218945
rs7218945
Entrez Id: 9611
Gene Symbol: NCOR1
NCOR1
CUI: C0428472
Disease:
Serum HDL cholesterol measurement
0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs7218945
rs7218945
Entrez Id: 9611
Gene Symbol: NCOR1
NCOR1
CUI: C0392885
Disease:
High density lipoprotein measurement
0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs7218945
rs7218945
Entrez Id: 9611
Gene Symbol: NCOR1
NCOR1
CUI: C0428474
Disease:
Serum LDL cholesterol measurement
0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs751569508
rs751569508
Entrez Id: 9611
Gene Symbol: NCOR1
NCOR1
CUI: C3810428
Disease:
Hyperlaxity
A 0.700 GeneticVariation CLINVAR
dbSNP: rs751569508
rs751569508
Entrez Id: 9611
Gene Symbol: NCOR1
NCOR1
CUI: C0557874
Disease:
Global developmental delay
A 0.700 GeneticVariation CLINVAR
dbSNP: rs751569508
rs751569508
Entrez Id: 9611
Gene Symbol: NCOR1
NCOR1
CUI: C0423757
Disease:
Thin skin
A 0.700 GeneticVariation CLINVAR
dbSNP: rs751569508
rs751569508
Entrez Id: 9611
Gene Symbol: NCOR1
NCOR1
CUI: C0424605
Disease:
Developmental delay (disorder)
A 0.700 GeneticVariation CLINVAR
dbSNP: rs751569508
rs751569508
Entrez Id: 9611
Gene Symbol: NCOR1
NCOR1
CUI: C0086437
Disease:
Joint laxity
A 0.700 GeneticVariation CLINVAR
dbSNP: rs71358386
rs71358386
Entrez Id: 9611
Gene Symbol: NCOR1
NCOR1
CUI: C0020179
Disease:
Huntington Disease
0.010 GeneticVariation BEFREE Two single-nucleotide polymorphisms (SNPs: rs71358386 in <i>NCOR1</i> and rs71358386 in <i>ADORA2B)</i> in the HD pathway were significantly associated with GM volume in the cuneus component, with minor alleles being linked to reduced GM volume. 29651271 2018
dbSNP: rs990933830
rs990933830
Entrez Id: 9611
Gene Symbol: NCOR1
NCOR1
CUI: C0028326
Disease:
Noonan Syndrome
0.010 GeneticVariation BEFREE A germline SOS1 mutation c.1310T>C (p. Ile437Thr) confirmed NS diagnosis. 30039904 2018