SFTA2, surfactant associated 2, 389376

N. diseases: 25; N. variants: 13
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2517449
rs2517449
Entrez Id: 135656;389376;102723346
Gene Symbol: MUCL3;SFTA2;HCG21
MUCL3;SFTA2;HCG21
CUI: C3853540
Disease:
Aspirin exacerbated respiratory disease 		0.010 GeneticVariation BEFREE After testing for multiple comparisons, only the association signal from rs2517449 was retained (P(corr) = .04), while other polymorphisms showed no associations with the risk of AERD and FEV(1) decline. 22152429 2012
dbSNP: rs3132581
rs3132581
Entrez Id: 135656;389376;102723346
Gene Symbol: MUCL3;SFTA2;HCG21
MUCL3;SFTA2;HCG21
CUI: C1263846
Disease:
Attention deficit hyperactivity disorder 		G 0.800 GeneticVariation GWASCAT Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. 23453885 2013
dbSNP: rs114115252
rs114115252
Entrez Id: 389376
Gene Symbol: SFTA2
SFTA2
CUI: C0036341
Disease:
Schizophrenia 		0.700 GeneticVariation GWASCAT Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia. 28540026 2017
dbSNP: rs114115252
rs114115252
Entrez Id: 389376
Gene Symbol: SFTA2
SFTA2
CUI: C0008074
Disease:
Child Development Disorders, Pervasive 		0.700 GeneticVariation GWASCAT Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia. 28540026 2017
dbSNP: rs114838832
rs114838832
Entrez Id: 135656;389376
Gene Symbol: MUCL3;SFTA2
MUCL3;SFTA2
CUI: C0036341
Disease:
Schizophrenia 		A 0.700 GeneticVariation GWASCAT Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia. 28540026 2017
dbSNP: rs114838832
rs114838832
Entrez Id: 135656;389376
Gene Symbol: MUCL3;SFTA2
MUCL3;SFTA2
CUI: C0008074
Disease:
Child Development Disorders, Pervasive 		A 0.700 GeneticVariation GWASCAT Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia. 28540026 2017
dbSNP: rs115123027
rs115123027
Entrez Id: 135656;389376
Gene Symbol: MUCL3;SFTA2
MUCL3;SFTA2
CUI: C0036341
Disease:
Schizophrenia 		T 0.700 GeneticVariation GWASCAT Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect. 30285260 2019
dbSNP: rs3132580
rs3132580
Entrez Id: 135656;389376;102723346
Gene Symbol: MUCL3;SFTA2;HCG21
MUCL3;SFTA2;HCG21
CUI: C0017665
Disease:
Membranous glomerulonephritis 		T 0.700 GeneticVariation GWASCAT Risk HLA-DQA1 and PLA(2)R1 alleles in idiopathic membranous nephropathy. 21323541 2011
dbSNP: rs3132581
rs3132581
Entrez Id: 135656;389376;102723346
Gene Symbol: MUCL3;SFTA2;HCG21
MUCL3;SFTA2;HCG21
CUI: C0008074
Disease:
Child Development Disorders, Pervasive 		G 0.700 GeneticVariation GWASCAT Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. 23453885 2013
dbSNP: rs3132581
rs3132581
Entrez Id: 135656;389376;102723346
Gene Symbol: MUCL3;SFTA2;HCG21
MUCL3;SFTA2;HCG21
CUI: C0005586
Disease:
Bipolar Disorder 		G 0.700 GeneticVariation GWASCAT Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. 23453885 2013
dbSNP: rs3132581
rs3132581
Entrez Id: 135656;389376;102723346
Gene Symbol: MUCL3;SFTA2;HCG21
MUCL3;SFTA2;HCG21
CUI: C1269683
Disease:
Major Depressive Disorder 		G 0.700 GeneticVariation GWASCAT Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. 23453885 2013
dbSNP: rs3132581
rs3132581
Entrez Id: 135656;389376;102723346
Gene Symbol: MUCL3;SFTA2;HCG21
MUCL3;SFTA2;HCG21
CUI: C0036341
Disease:
Schizophrenia 		G 0.700 GeneticVariation GWASCAT Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. 23453885 2013
dbSNP: rs3132581
rs3132581
Entrez Id: 135656;389376;102723346
Gene Symbol: MUCL3;SFTA2;HCG21
MUCL3;SFTA2;HCG21
CUI: C1263846
Disease:
Attention deficit hyperactivity disorder 		G 0.800 GeneticVariation GWASDB Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. 23453885 2013
dbSNP: rs12190030
rs12190030
Entrez Id: 135656;389376;102723346
Gene Symbol: MUCL3;SFTA2;HCG21
MUCL3;SFTA2;HCG21
CUI: C1836232
Disease:
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.700 GeneticVariation GWASDB The major genetic determinants of HIV-1 control affect HLA class I peptide presentation. 21051598 2010
dbSNP: rs12190030
rs12190030
Entrez Id: 135656;389376;102723346
Gene Symbol: MUCL3;SFTA2;HCG21
MUCL3;SFTA2;HCG21
CUI: C1836231
Disease:
HIV-1, RESISTANCE TO 		0.700 GeneticVariation GWASDB The major genetic determinants of HIV-1 control affect HLA class I peptide presentation. 21051598 2010
dbSNP: rs12190030
rs12190030
Entrez Id: 135656;389376;102723346
Gene Symbol: MUCL3;SFTA2;HCG21
MUCL3;SFTA2;HCG21
CUI: C1836233
Disease:
AIDS, PROGRESSION TO 		0.700 GeneticVariation GWASDB The major genetic determinants of HIV-1 control affect HLA class I peptide presentation. 21051598 2010
dbSNP: rs12190030
rs12190030
Entrez Id: 135656;389376;102723346
Gene Symbol: MUCL3;SFTA2;HCG21
MUCL3;SFTA2;HCG21
CUI: C1836230
Disease:
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.700 GeneticVariation GWASDB The major genetic determinants of HIV-1 control affect HLA class I peptide presentation. 21051598 2010
dbSNP: rs12697941
rs12697941
Entrez Id: 135656;389376
Gene Symbol: MUCL3;SFTA2
MUCL3;SFTA2
CUI: C1836233
Disease:
AIDS, PROGRESSION TO 		0.700 GeneticVariation GWASDB Common genetic variation and the control of HIV-1 in humans. 20041166 2009
dbSNP: rs12697941
rs12697941
Entrez Id: 135656;389376
Gene Symbol: MUCL3;SFTA2
MUCL3;SFTA2
CUI: C1836231
Disease:
HIV-1, RESISTANCE TO 		0.700 GeneticVariation GWASDB Common genetic variation and the control of HIV-1 in humans. 20041166 2009
dbSNP: rs12697941
rs12697941
Entrez Id: 135656;389376
Gene Symbol: MUCL3;SFTA2
MUCL3;SFTA2
CUI: C1836230
Disease:
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.700 GeneticVariation GWASDB Common genetic variation and the control of HIV-1 in humans. 20041166 2009
dbSNP: rs12697941
rs12697941
Entrez Id: 135656;389376
Gene Symbol: MUCL3;SFTA2
MUCL3;SFTA2
CUI: C1836232
Disease:
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.700 GeneticVariation GWASDB Common genetic variation and the control of HIV-1 in humans. 20041166 2009
dbSNP: rs2240804
rs2240804
Entrez Id: 135656;389376;102723346
Gene Symbol: MUCL3;SFTA2;HCG21
MUCL3;SFTA2;HCG21
CUI: C0003873
Disease:
Rheumatoid Arthritis 		0.700 GeneticVariation GWASDB TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study. 17804836 2007
dbSNP: rs2240804
rs2240804
Entrez Id: 135656;389376;102723346
Gene Symbol: MUCL3;SFTA2;HCG21
MUCL3;SFTA2;HCG21
CUI: C0003873
Disease:
Rheumatoid Arthritis 		0.700 GeneticVariation GWASDB REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis. 19503088 2009
dbSNP: rs2253705
rs2253705
Entrez Id: 389376
Gene Symbol: SFTA2
SFTA2
CUI: C0019163
Disease:
Hepatitis B 		0.700 GeneticVariation GWASDB A genome-wide association study identified new variants associated with the risk of chronic hepatitis B. 23760081 2013
dbSNP: rs3132571
rs3132571
Entrez Id: 135656;389376
Gene Symbol: MUCL3;SFTA2
MUCL3;SFTA2
CUI: C0011854
Disease:
Diabetes Mellitus, Insulin-Dependent 		0.700 GeneticVariation GWASDB A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene. 17632545 2007