ARMC2, armadillo repeat containing 2, 84071

N. diseases: 21; N. variants: 28
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2798641
rs2798641
Entrez Id: 84071
Gene Symbol: ARMC2
ARMC2
CUI: C0016529
Disease:
Forced expiratory volume function 		T 0.800 GeneticVariation GWASCAT New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. 30804560 2019
dbSNP: rs2798641
rs2798641
Entrez Id: 84071
Gene Symbol: ARMC2
ARMC2
CUI: C0016529
Disease:
Forced expiratory volume function 		0.800 GeneticVariation GWASDB Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function. 23284291 2012
dbSNP: rs2798641
rs2798641
Entrez Id: 84071
Gene Symbol: ARMC2
ARMC2
CUI: C0016529
Disease:
Forced expiratory volume function 		0.800 GeneticVariation GWASCAT Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function. 23284291 2012
dbSNP: rs118126621
rs118126621
Entrez Id: 84071
Gene Symbol: ARMC2
ARMC2
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1268055
rs1268055
Entrez Id: 84071
Gene Symbol: ARMC2
ARMC2
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1562332833
rs1562332833
Entrez Id: 84071
Gene Symbol: ARMC2
ARMC2
CUI: C4706677
Disease:
Male infertility with teratozoospermia due to single gene mutation 		T 0.700 CausalMutation CLINVAR Bi-allelic Mutations in ARMC2 Lead to Severe Astheno-Teratozoospermia Due to Sperm Flagellum Malformations in Humans and Mice. 30686508 2019
dbSNP: rs1562372417
rs1562372417
Entrez Id: 84071
Gene Symbol: ARMC2
ARMC2
CUI: C4706677
Disease:
Male infertility with teratozoospermia due to single gene mutation 		A 0.700 CausalMutation CLINVAR Bi-allelic Mutations in ARMC2 Lead to Severe Astheno-Teratozoospermia Due to Sperm Flagellum Malformations in Humans and Mice. 30686508 2019
dbSNP: rs1562381747
rs1562381747
Entrez Id: 84071;101929716
Gene Symbol: ARMC2;ARMC2-AS1
ARMC2;ARMC2-AS1
CUI: C4706677
Disease:
Male infertility with teratozoospermia due to single gene mutation 		T 0.700 CausalMutation CLINVAR Bi-allelic Mutations in ARMC2 Lead to Severe Astheno-Teratozoospermia Due to Sperm Flagellum Malformations in Humans and Mice. 30686508 2019
dbSNP: rs1562435988
rs1562435988
Entrez Id: 84071
Gene Symbol: ARMC2
ARMC2
CUI: C4706677
Disease:
Male infertility with teratozoospermia due to single gene mutation 		A 0.700 CausalMutation CLINVAR Bi-allelic Mutations in ARMC2 Lead to Severe Astheno-Teratozoospermia Due to Sperm Flagellum Malformations in Humans and Mice. 30686508 2019
dbSNP: rs1562436860
rs1562436860
Entrez Id: 84071
Gene Symbol: ARMC2
ARMC2
CUI: C4706677
Disease:
Male infertility with teratozoospermia due to single gene mutation 		C 0.700 CausalMutation CLINVAR Bi-allelic Mutations in ARMC2 Lead to Severe Astheno-Teratozoospermia Due to Sperm Flagellum Malformations in Humans and Mice. 30686508 2019
dbSNP: rs2798641
rs2798641
Entrez Id: 84071
Gene Symbol: ARMC2
ARMC2
CUI: C1518922
Disease:
peak expiratory flow (procedure) 		T 0.700 GeneticVariation GWASCAT New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. 30804560 2019
dbSNP: rs2806356
rs2806356
Entrez Id: 84071
Gene Symbol: ARMC2
ARMC2
CUI: C0024117
Disease:
Chronic Obstructive Airway Disease 		C 0.700 GeneticVariation GWASCAT Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations. 30804561 2019
dbSNP: rs6568554
rs6568554
Entrez Id: 84071
Gene Symbol: ARMC2
ARMC2
CUI: C0005612
Disease:
Birth Weight 		A 0.700 GeneticVariation GWASCAT Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors. 31043758 2019
dbSNP: rs76094073
rs76094073
Entrez Id: 84071
Gene Symbol: ARMC2
ARMC2
CUI: C0005612
Disease:
Birth Weight 		G 0.700 GeneticVariation GWASCAT Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors. 31043758 2019
dbSNP: rs2273669
rs2273669
Entrez Id: 84071
Gene Symbol: ARMC2
ARMC2
CUI: C0600139
Disease:
Prostate carcinoma 		G 0.700 GeneticVariation GWASCAT Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci. 29892016 2018
dbSNP: rs2806356
rs2806356
Entrez Id: 84071
Gene Symbol: ARMC2
ARMC2
CUI: C0024117
Disease:
Chronic Obstructive Airway Disease 		C 0.700 GeneticVariation GWASCAT Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosis. 28166215 2017
dbSNP: rs11153147
rs11153147
Entrez Id: 84071
Gene Symbol: ARMC2
ARMC2
CUI: C0524587
Disease:
Mean Corpuscular Volume (result) 		G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs2273669
rs2273669
Entrez Id: 84071
Gene Symbol: ARMC2
ARMC2
CUI: C0376358
Disease:
Malignant neoplasm of prostate 		G 0.700 GeneticVariation GWASDB Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array. 23535732 2013
dbSNP: rs2273669
rs2273669
Entrez Id: 84071
Gene Symbol: ARMC2
ARMC2
CUI: C0600139
Disease:
Prostate carcinoma 		G 0.700 GeneticVariation GWASCAT Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array. 23535732 2013
dbSNP: rs11754955
rs11754955
Entrez Id: 84071
Gene Symbol: ARMC2
ARMC2
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs12193858
rs12193858
Entrez Id: 84071
Gene Symbol: ARMC2
ARMC2
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs12195378
rs12195378
Entrez Id: 84071
Gene Symbol: ARMC2
ARMC2
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs12195728
rs12195728
Entrez Id: 84071
Gene Symbol: ARMC2
ARMC2
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs12195848
rs12195848
Entrez Id: 84071
Gene Symbol: ARMC2
ARMC2
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs12196010
rs12196010
Entrez Id: 84071
Gene Symbol: ARMC2
ARMC2
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012