Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs119476044
rs119476044
Entrez Id: 54583
Gene Symbol: EGLN1
EGLN1
CUI: C1853286
Disease:
Erythrocytosis, Familial, 3
0.800 GeneticVariation UNIPROT Clinical utility gene card for: familial erythrocytosis. 22274579 2012
dbSNP: rs80358193
rs80358193
Entrez Id: 54583
Gene Symbol: EGLN1
EGLN1
CUI: C1853286
Disease:
Erythrocytosis, Familial, 3
0.800 GeneticVariation UNIPROT Clinical utility gene card for: familial erythrocytosis. 22274579 2012
dbSNP: rs80358193
rs80358193
Entrez Id: 54583
Gene Symbol: EGLN1
EGLN1
CUI: C1853286
Disease:
Erythrocytosis, Familial, 3
0.800 GeneticVariation UNIPROT A novel erythrocytosis-associated PHD2 mutation suggests the location of a HIF binding groove. 17579185 2007
dbSNP: rs80358193
rs80358193
Entrez Id: 54583
Gene Symbol: EGLN1
EGLN1
CUI: C1853286
Disease:
Erythrocytosis, Familial, 3
0.800 GeneticVariation UNIPROT A family with erythrocytosis establishes a role for prolyl hydroxylase domain protein 2 in oxygen homeostasis. 16407130 2006
dbSNP: rs119476044
rs119476044
Entrez Id: 54583
Gene Symbol: EGLN1
EGLN1
CUI: C1853286
Disease:
Erythrocytosis, Familial, 3
T 0.800 CausalMutation CLINVAR
dbSNP: rs80358193
rs80358193
Entrez Id: 54583
Gene Symbol: EGLN1
EGLN1
CUI: C1853286
Disease:
Erythrocytosis, Familial, 3
C 0.800 CausalMutation CLINVAR
dbSNP: rs61835223
rs61835223
Entrez Id: 54583
Gene Symbol: EGLN1
EGLN1
CUI: C0014772
Disease:
Red Blood Cell Count measurement
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs508618
rs508618
Entrez Id: 54583
Gene Symbol: EGLN1
EGLN1
CUI: C0014772
Disease:
Red Blood Cell Count measurement
A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs533281866
rs533281866
Entrez Id: 54583
Gene Symbol: EGLN1
EGLN1
CUI: C0518015
Disease:
Hemoglobin measurement
C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs533281866
rs533281866
Entrez Id: 54583
Gene Symbol: EGLN1
EGLN1
CUI: C0018935
Disease:
Hematocrit procedure
C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs533281866
rs533281866
Entrez Id: 54583
Gene Symbol: EGLN1
EGLN1
CUI: C0014772
Disease:
Red Blood Cell Count measurement
C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs576195416
rs576195416
Entrez Id: 54583
Gene Symbol: EGLN1
EGLN1
CUI: C0018935
Disease:
Hematocrit procedure
AT 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs119476045
rs119476045
Entrez Id: 54583
Gene Symbol: EGLN1
EGLN1
CUI: C1853286
Disease:
Erythrocytosis, Familial, 3
C 0.700 CausalMutation CLINVAR
dbSNP: rs80358193
rs80358193
Entrez Id: 54583
Gene Symbol: EGLN1
EGLN1
CUI: C0152264
Disease:
Familial erythrocytosis
0.020 GeneticVariation BEFREE Recently, a missense mutation [c.950C>G (p.Pro317Arg)] in the prolyl hydroxylase domain protein 2 (PHD2) gene, whose encoded protein has HIF-1alpha as a substrate, provided evidence of the PHD2 role in a case of familial erythrocytosis. 17933562 2008
dbSNP: rs80358193
rs80358193
Entrez Id: 54583
Gene Symbol: EGLN1
EGLN1
CUI: C4551637
Disease:
Erythrocytosis familial, 1
0.020 GeneticVariation BEFREE Herein, we examine the biochemical characterization of PHD2 variants, Arg371His and Pro317Arg, identified from patients with familial erythrocytosis. 18834144 2008
dbSNP: rs80358193
rs80358193
Entrez Id: 54583
Gene Symbol: EGLN1
EGLN1
CUI: C4551637
Disease:
Erythrocytosis familial, 1
0.020 GeneticVariation BEFREE Recently, a missense mutation [c.950C>G (p.Pro317Arg)] in the prolyl hydroxylase domain protein 2 (PHD2) gene, whose encoded protein has HIF-1alpha as a substrate, provided evidence of the PHD2 role in a case of familial erythrocytosis. 17933562 2008
dbSNP: rs80358193
rs80358193
Entrez Id: 54583
Gene Symbol: EGLN1
EGLN1
CUI: C0152264
Disease:
Familial erythrocytosis
0.020 GeneticVariation BEFREE Herein, we examine the biochemical characterization of PHD2 variants, Arg371His and Pro317Arg, identified from patients with familial erythrocytosis. 18834144 2008
dbSNP: rs12097901
rs12097901
Entrez Id: 54583
Gene Symbol: EGLN1
EGLN1
CUI: C0684249
Disease:
Carcinoma of lung
0.010 GeneticVariation BEFREE We observed a significant association between the selected Tibetan EGLN1/PHD2 haplotype and lung cancer (p=0.0012 for D4E, p=0.0002 for C127S), corresponding to a two-fold increase in lung cancer risk. 28036300 2017
dbSNP: rs12097901
rs12097901
Entrez Id: 54583
Gene Symbol: EGLN1
EGLN1
CUI: C1306460
Disease:
Primary malignant neoplasm of lung
0.010 GeneticVariation BEFREE We observed a significant association between the selected Tibetan EGLN1/PHD2 haplotype and lung cancer (p=0.0012 for D4E, p=0.0002 for C127S), corresponding to a two-fold increase in lung cancer risk. 28036300 2017
dbSNP: rs12097901
rs12097901
Entrez Id: 54583
Gene Symbol: EGLN1
EGLN1
CUI: C0242379
Disease:
Malignant neoplasm of lung
0.010 GeneticVariation BEFREE We observed a significant association between the selected Tibetan EGLN1/PHD2 haplotype and lung cancer (p=0.0012 for D4E, p=0.0002 for C127S), corresponding to a two-fold increase in lung cancer risk. 28036300 2017
dbSNP: rs516651
rs516651
Entrez Id: 54583
Gene Symbol: EGLN1
EGLN1
CUI: C0035222
Disease:
Respiratory Distress Syndrome, Adult
0.010 GeneticVariation BEFREE <i>PHD2</i> rs516651 TT-genotype in ARDS was independently associated with a 3.34 times greater mortality risk (OR 3.34, CI 1.09-10.22; <i>p</i> = 0.034) within 30-days, whereas the other SNPs had no significant impact (<i>p</i> = ns). 28613249 2017
dbSNP: rs480902
rs480902
Entrez Id: 54583
Gene Symbol: EGLN1
EGLN1
CUI: C0340100
Disease:
High altitude pulmonary edema
0.010 GeneticVariation BEFREE Statistical analyses of the genotype frequencies of the SNPs revealed significant differences in the ACE (rs4309), EGLN1 (rs480902), SP-A2 (rs1965708), HSP70 (rs1008438), PAI-1 (rs1799889), and NOS (rs199983) expressions between the HAPE and healthy control groups (P < 0.05); therefore, these SNP loci were believed to indicate HAPE susceptibility. 26436397 2015
dbSNP: rs12097901
rs12097901
Entrez Id: 54583
Gene Symbol: EGLN1
EGLN1
CUI: C0032461
Disease:
Polycythemia
0.010 GeneticVariation BEFREE The c.[12C>G; 380G>C] mutation abrogates hypoxia-induced and HIF-mediated augmentation of erythropoiesis, which provides a molecular mechanism for the observed protection of Tibetans from polycythemia at high altitude. 25129147 2014
dbSNP: rs12406290
rs12406290
Entrez Id: 54583
Gene Symbol: EGLN1
EGLN1
CUI: C1860224
Disease:
ABLEPHARON-MACROSTOMIA SYNDROME
0.010 GeneticVariation BEFREE Carriers of the "GG" haplotype of rs12406290-rs2153364 exhibited an increased risk of AMS after adjustments for age and smoking status. 25431923 2014
dbSNP: rs12757362
rs12757362
Entrez Id: 54583
Gene Symbol: EGLN1
EGLN1
CUI: C1860224
Disease:
ABLEPHARON-MACROSTOMIA SYNDROME
0.010 GeneticVariation BEFREE No significant association was noted between AMS and rs12757362, rs1339894, rs1361384, rs2009873, rs2739513 or rs2486729 before and after Bonferroni correction. 25431923 2014