MYRF, myelin regulatory factor, 745

N. diseases: 102; N. variants: 44
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs174537
rs174537
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C0202236
Disease:
Triglycerides measurement
T 0.800 GeneticVariation GWASCAT Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program. 30275531 2018
dbSNP: rs174537
rs174537
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C0009402
Disease:
Colorectal Carcinoma
G 0.800 GeneticVariation GWASCAT Identification of Susceptibility Loci and Genes for Colorectal Cancer Risk. 26965516 2016
dbSNP: rs174537
rs174537
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C0009402
Disease:
Colorectal Carcinoma
G 0.800 GeneticVariation GWASCAT Large-Scale Genome-Wide Association Study of East Asians Identifies Loci Associated With Risk for Colorectal Cancer. 30529582 2019
dbSNP: rs174537
rs174537
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C0009402
Disease:
Colorectal Carcinoma
G 0.800 GeneticVariation GWASCAT Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer risk. 24836286 2014
dbSNP: rs108499
rs108499
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB Genome-wide association study identifies multiple loci influencing human serum metabolite levels. 22286219 2012
dbSNP: rs108499
rs108499
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C0202177
Disease:
Phospholipid measurement
0.700 GeneticVariation GWASDB Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium. 21829377 2011
dbSNP: rs108499
rs108499
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs11320420
rs11320420
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C1561643
Disease:
Chronic Kidney Diseases
G 0.700 GeneticVariation GWASCAT Genome-Wide Association Studies of Metabolites in Patients with CKD Identify Multiple Loci and Illuminate Tubular Transport Mechanisms. 29545352 2018
dbSNP: rs11320420
rs11320420
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C0022661
Disease:
Kidney Failure, Chronic
G 0.700 GeneticVariation GWASCAT Genome-Wide Association Studies of Metabolites in Patients with CKD Identify Multiple Loci and Illuminate Tubular Transport Mechanisms. 29545352 2018
dbSNP: rs149803
rs149803
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB Genome-wide association study identifies multiple loci influencing human serum metabolite levels. 22286219 2012
dbSNP: rs149803
rs149803
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C0202177
Disease:
Phospholipid measurement
0.700 GeneticVariation GWASDB Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium. 21829377 2011
dbSNP: rs149804
rs149804
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB Genome-wide association study identifies multiple loci influencing human serum metabolite levels. 22286219 2012
dbSNP: rs1565295267
rs1565295267
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C1735886
Disease:
Bland White Garland Syndrome
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1565295267
rs1565295267
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C0010417
Disease:
Cryptorchidism
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1565295267
rs1565295267
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C0032461
Disease:
Polycythemia
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1565295267
rs1565295267
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C4551904
Disease:
Total Anomalous Pulmonary Venous Return 1
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1565295267
rs1565295267
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C0240635
Disease:
Byzanthine arch palate
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1565295267
rs1565295267
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C0011813
Disease:
Dextrocardia
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1565295286
rs1565295286
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C4722446
Disease:
ENCEPHALITIS/ENCEPHALOPATHY, MILD, WITH REVERSIBLE MYELIN VACUOLIZATION
G 0.700 CausalMutation CLINVAR
dbSNP: rs1565295395
rs1565295395
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C4748946
Disease:
CARDIAC-UROGENITAL SYNDROME
AAG 0.700 CausalMutation CLINVAR
dbSNP: rs1565295550
rs1565295550
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C4748946
Disease:
CARDIAC-UROGENITAL SYNDROME
A 0.700 CausalMutation CLINVAR
dbSNP: rs1565304230
rs1565304230
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C4748946
Disease:
CARDIAC-UROGENITAL SYNDROME
T 0.700 CausalMutation CLINVAR
dbSNP: rs1565307564
rs1565307564
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C0018817
Disease:
Atrial Septal Defects
G 0.700 CausalMutation CLINVAR
dbSNP: rs1565307564
rs1565307564
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C4748946
Disease:
CARDIAC-UROGENITAL SYNDROME
G 0.700 CausalMutation CLINVAR
dbSNP: rs1565307564
rs1565307564
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C0013274
Disease:
Patent ductus arteriosus
G 0.700 CausalMutation CLINVAR