ARG2, arginase 2, 384

N. diseases: 103; N. variants: 4
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3742879
rs3742879
Entrez Id: 384;10243;10490
Gene Symbol: ARG2;GPHN;VTI1B
ARG2;GPHN;VTI1B
CUI: C0004096
Disease:
Asthma 		0.020 GeneticVariation BEFREE The association of a NOS2A promoter haplotype with FeNO varied significantly by rs3742879 genotypes and by ast</span>hma. 21039601 2011
dbSNP: rs3742879
rs3742879
Entrez Id: 384;10243;10490
Gene Symbol: ARG2;GPHN;VTI1B
ARG2;GPHN;VTI1B
CUI: C0004096
Disease:
Asthma 		0.020 GeneticVariation BEFREE Two polymorphisms in arginase 2 (rs17249437 and rs3742879) were associated with asthma and with more severe airway obstruction. 20124949 2010
dbSNP: rs15493
rs15493
Entrez Id: 384;10243;10490
Gene Symbol: ARG2;GPHN;VTI1B
ARG2;GPHN;VTI1B
CUI: C0041327
Disease:
Tuberculosis, Pulmonary 		0.010 GeneticVariation BEFREE However, the <i>VTI1B</i> rs15493 SNP had no impact on the susceptibility to PTB (<i>p</i> > 0.05). 30945947 2019
dbSNP: rs17249437
rs17249437
Entrez Id: 384;10243
Gene Symbol: ARG2;GPHN
ARG2;GPHN
CUI: C0001883
Disease:
Airway Obstruction 		0.010 GeneticVariation BEFREE Two polymorphisms in arginase 2 (rs17249437 and rs3742879) were associated with asthma and with more severe airway obstruction. 20124949 2010
dbSNP: rs17249437
rs17249437
Entrez Id: 384;10243
Gene Symbol: ARG2;GPHN
ARG2;GPHN
CUI: C0004096
Disease:
Asthma 		0.010 GeneticVariation BEFREE Two polymorphisms in arginase 2 (rs17249437 and rs3742879) were associated with asthma and with more severe airway obstruction. 20124949 2010
dbSNP: rs3742879
rs3742879
Entrez Id: 384;10243;10490
Gene Symbol: ARG2;GPHN;VTI1B
ARG2;GPHN;VTI1B
CUI: C0001883
Disease:
Airway Obstruction 		0.010 GeneticVariation BEFREE Two polymorphisms in arginase 2 (rs17249437 and rs3742879) were associated with asthma and with more severe airway obstruction. 20124949 2010
dbSNP: rs742869
rs742869
Entrez Id: 384;10243
Gene Symbol: ARG2;GPHN
ARG2;GPHN
CUI: C0002395
Disease:
Alzheimer's Disease 		0.010 GeneticVariation BEFREE The presence of the rare arginase 2 allele rs742869 was associated with an increase in the risk of AD in men and with an earlier age-at-onset for both genders. 20693631 2010