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: rs10792318
rs10792318
Entrez Id: 745
Gene Symbol: MYRF
MYRF
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: rs11230796
rs11230796
Entrez Id: 745
Gene Symbol: MYRF
MYRF
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: rs1565286228
rs1565286228
Entrez Id: 745
Gene Symbol: MYRF
MYRF
CUI: C1691215
Disease:
Penile hypospadias 		T 0.700 CausalMutation CLINVAR
dbSNP: rs1565286228
rs1565286228
Entrez Id: 745
Gene Symbol: MYRF
MYRF
CUI: C0266362
Disease:
Ambiguous Genitalia 		T 0.700 CausalMutation CLINVAR
dbSNP: rs1565286228
rs1565286228
Entrez Id: 745
Gene Symbol: MYRF
MYRF
CUI: C0020295
Disease:
Hydronephrosis 		T 0.700 CausalMutation CLINVAR
dbSNP: rs1565286228
rs1565286228
Entrez Id: 745
Gene Symbol: MYRF
MYRF
CUI: C4748946
Disease:
CARDIAC-UROGENITAL SYNDROME 		T 0.700 CausalMutation CLINVAR
dbSNP: rs1565286228
rs1565286228
Entrez Id: 745
Gene Symbol: MYRF
MYRF
CUI: C0235833
Disease:
Congenital diaphragmatic hernia 		T 0.700 CausalMutation CLINVAR
dbSNP: rs1565286228
rs1565286228
Entrez Id: 745
Gene Symbol: MYRF
MYRF
CUI: C0221353
Disease:
Horseshoe Kidney 		T 0.700 CausalMutation CLINVAR
dbSNP: rs198467
rs198467
Entrez Id: 745
Gene Symbol: MYRF
MYRF
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: rs2071213
rs2071213
Entrez Id: 745
Gene Symbol: MYRF
MYRF
CUI: C2931384
Disease:
Moyamoya disease 1 		A 0.700 GeneticVariation GWASCAT Novel Susceptibility Loci for Moyamoya Disease Revealed by a Genome-Wide Association Study. 29273593 2018
dbSNP: rs2071213
rs2071213
Entrez Id: 745
Gene Symbol: MYRF
MYRF
CUI: C0026654
Disease:
Moyamoya Disease 		A 0.700 GeneticVariation GWASCAT Novel Susceptibility Loci for Moyamoya Disease Revealed by a Genome-Wide Association Study. 29273593 2018
dbSNP: rs547589
rs547589
Entrez Id: 745
Gene Symbol: MYRF
MYRF
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: rs55903902
rs55903902
Entrez Id: 745
Gene Symbol: MYRF
MYRF
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: rs198421
rs198421
Entrez Id: 745;26070
Gene Symbol: MYRF;MYRF-AS1
MYRF;MYRF-AS1
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: rs198459
rs198459
Entrez Id: 745;26070
Gene Symbol: MYRF;MYRF-AS1
MYRF;MYRF-AS1
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: rs198462
rs198462
Entrez Id: 745;26070
Gene Symbol: MYRF;MYRF-AS1
MYRF;MYRF-AS1
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: rs198464
rs198464
Entrez Id: 745;26070
Gene Symbol: MYRF;MYRF-AS1
MYRF;MYRF-AS1
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: rs198476
rs198476
Entrez Id: 745;26070
Gene Symbol: MYRF;MYRF-AS1
MYRF;MYRF-AS1
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: rs2956395
rs2956395
Entrez Id: 745;26070
Gene Symbol: MYRF;MYRF-AS1
MYRF;MYRF-AS1
CUI: C0005586
Disease:
Bipolar Disorder 		C 0.700 GeneticVariation GWASCAT Genome-wide association study identifies 30 loci associated with bipolar disorder. 31043756 2019
dbSNP: rs569258
rs569258
Entrez Id: 745;26070
Gene Symbol: MYRF;MYRF-AS1
MYRF;MYRF-AS1
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: rs1382225004
rs1382225004
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C4748946
Disease:
CARDIAC-UROGENITAL SYNDROME 		0.800 GeneticVariation UNIPROT
dbSNP: rs1382225004
rs1382225004
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C4748946
Disease:
CARDIAC-UROGENITAL SYNDROME 		A 0.800 CausalMutation CLINVAR
dbSNP: rs174537
rs174537
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C0009402
Disease:
Colorectal Carcinoma 		G 0.800 GeneticVariation GWASCAT GWAS identifies two novel colorectal cancer loci at 16q24.1 and 20q13.12. 29471430 2018
dbSNP: rs174537
rs174537
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C0009402
Disease:
Colorectal Carcinoma 		G 0.800 GeneticVariation GWASDB Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer risk. 24836286 2014
dbSNP: rs174537
rs174537
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C0202236
Disease:
Triglycerides measurement 		0.800 GeneticVariation GWASDB A null mutation in human APOC3 confers a favorable plasma lipid profile and apparent cardioprotection. 19074352 2008