SPATA13, spermatogenesis associated 13, 221178

N. diseases: 15; N. variants: 5
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs715921
rs715921
Entrez Id: 221178
Gene Symbol: SPATA13
SPATA13
CUI: C0035227
Disease:
Respiratory Function Tests 		A 0.800 GeneticVariation GWASDB Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction. 22837378 2012
dbSNP: rs715921
rs715921
Entrez Id: 221178
Gene Symbol: SPATA13
SPATA13
CUI: C0035227
Disease:
Respiratory Function Tests 		A 0.800 GeneticVariation GWASCAT Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction. 22837378 2012
dbSNP: rs9507287
rs9507287
Entrez Id: 221178
Gene Symbol: SPATA13
SPATA13
CUI: C0004364
Disease:
Autoimmune Diseases 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs9507287
rs9507287
Entrez Id: 221178
Gene Symbol: SPATA13
SPATA13
CUI: C3150797
Disease:
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs9507287
rs9507287
Entrez Id: 221178
Gene Symbol: SPATA13
SPATA13
CUI: C0020676
Disease:
Hypothyroidism 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs9507287
rs9507287
Entrez Id: 221178
Gene Symbol: SPATA13
SPATA13
CUI: C4310768
Disease:
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs9507287
rs9507287
Entrez Id: 221178
Gene Symbol: SPATA13
SPATA13
CUI: C4014795
Disease:
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs7329958
rs7329958
Entrez Id: 221178
Gene Symbol: SPATA13
SPATA13
CUI: C0202230
Disease:
Thyroid stimulating hormone measurement 		T 0.700 GeneticVariation GWASCAT Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation. 30367059 2018
dbSNP: rs9511143
rs9511143
Entrez Id: 221178
Gene Symbol: SPATA13
SPATA13
CUI: C0020676
Disease:
Hypothyroidism 		0.700 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965 2016
dbSNP: rs1220597
rs1220597
Entrez Id: 221178
Gene Symbol: SPATA13
SPATA13
CUI: C1337013
Disease:
Differentiated Thyroid Gland Carcinoma 		0.010 GeneticVariation BEFREE A possible role in DTC susceptibility in the Italian populations was also found for rs13184587 (ARSB) (P = 8.54 × 10(-6)) and rs1220597 (SPATA13) (P = 3.25 × 10(-6)). 25029422 2014
dbSNP: rs1220597
rs1220597
Entrez Id: 221178
Gene Symbol: SPATA13
SPATA13
CUI: C4722172
Disease:
Primary differentiated carcinoma of thyroid gland 		0.010 GeneticVariation BEFREE A possible role in DTC susceptibility in the Italian populations was also found for rs13184587 (ARSB) (P = 8.54 × 10(-6)) and rs1220597 (SPATA13) (P = 3.25 × 10(-6)). 25029422 2014