NCOA1, nuclear receptor coactivator 1, 8648

N. diseases: 108; N. variants: 7
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10865308
rs10865308
Entrez Id: 8648
Gene Symbol: NCOA1
NCOA1
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs188671617
rs188671617
Entrez Id: 8648
Gene Symbol: NCOA1
NCOA1
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2044148
rs2044148
Entrez Id: 8648
Gene Symbol: NCOA1
NCOA1
CUI: C1305855
Disease:
Body mass index 		G 0.700 GeneticVariation GWASCAT A Large Multiethnic Genome-Wide Association Study of Adult Body Mass Index Identifies Novel Loci. 30108127 2018
dbSNP: rs200648189
rs200648189
Entrez Id: 8648
Gene Symbol: NCOA1
NCOA1
CUI: C0678222
Disease:
Breast Carcinoma 		CT 0.700 GeneticVariation GWASCAT Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer. 29058716 2017
dbSNP: rs2044148
rs2044148
Entrez Id: 8648
Gene Symbol: NCOA1
NCOA1
CUI: C4049938
Disease:
Physical Activity Measurement 		A 0.700 GeneticVariation GWASCAT Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults. 28448500 2017
dbSNP: rs55783347
rs55783347
Entrez Id: 8648
Gene Symbol: NCOA1
NCOA1
CUI: C0021704
Disease:
Intelligence 		0.700 GeneticVariation GWASCAT GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium. 28093568 2017
dbSNP: rs6545667
rs6545667
Entrez Id: 8648
Gene Symbol: NCOA1
NCOA1
CUI: C0202236
Disease:
Triglycerides measurement 		0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs7572475
rs7572475
Entrez Id: 8648
Gene Symbol: NCOA1
NCOA1
CUI: C1842937
Disease:
AURAL ATRESIA, CONGENITAL 		0.010 GeneticVariation BEFREE We investigated four SRC-1 gene polymorphisms (rs11894248, rs17791703, rs7572475, and rs9309308) and their correlation with KD with CAA susceptibility in 327 Taiwanese people (279 KD patients without CAA and 48 KD patients with CAA). 24652666 2014
dbSNP: rs7572475
rs7572475
Entrez Id: 8648
Gene Symbol: NCOA1
NCOA1
CUI: C0026691
Disease:
Mucocutaneous Lymph Node Syndrome 		0.010 GeneticVariation BEFREE We investigated four SRC-1 gene polymorphisms (rs11894248, rs17791703, rs7572475, and rs9309308) and their correlation with KD with CAA susceptibility in 327 Taiwanese people (279 KD patients without CAA and 48 KD patients with CAA). 24652666 2014