VRTN, vertebrae development associated, 55237

N. diseases: 3; N. variants: 2
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10141786
rs10141786
Entrez Id: 55237
Gene Symbol: VRTN
VRTN
CUI: C0016529
Disease:
Forced expiratory volume function 		A 0.700 GeneticVariation GWASCAT New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. 30804560 2019
dbSNP: rs10141786
rs10141786
Entrez Id: 55237
Gene Symbol: VRTN
VRTN
CUI: C0042834
Disease:
Vital capacity 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs10141786
rs10141786
Entrez Id: 55237
Gene Symbol: VRTN
VRTN
CUI: C0042834
Disease:
Vital capacity 		A 0.700 GeneticVariation GWASCAT New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. 30804560 2019
dbSNP: rs773509797
rs773509797
Entrez Id: 55237
Gene Symbol: VRTN
VRTN
CUI: C0009402
Disease:
Colorectal Carcinoma 		0.700 GeneticVariation UNIPROT