MYH7B, myosin heavy chain 7B, 57644

N. diseases: 18; N. variants: 20
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1885120
rs1885120
Entrez Id: 57644;574501;107985393
Gene Symbol: MYH7B;MIR499A;LOC107985393
MYH7B;MIR499A;LOC107985393
CUI: C0025202
Disease:
melanoma 		C 0.800 GeneticVariation GWASCAT Two-stage genome-wide association study identifies a novel susceptibility locus associated with melanoma. 28212542 2017
dbSNP: rs17310467
rs17310467
Entrez Id: 2937;57644
Gene Symbol: GSS;MYH7B
GSS;MYH7B
CUI: C0919677
Disease:
Protein C measurement 		0.800 GeneticVariation GWASDB Genome wide association study for plasma levels of natural anticoagulant inhibitors and protein C anticoagulant pathway: the MARTHA project. 22443383 2012
dbSNP: rs17310467
rs17310467
Entrez Id: 2937;57644
Gene Symbol: GSS;MYH7B
GSS;MYH7B
CUI: C1168438
Disease:
Protein C antigen measurement 		0.800 GeneticVariation GWASCAT Genome wide association study for plasma levels of natural anticoagulant inhibitors and protein C anticoagulant pathway: the MARTHA project. 22443383 2012
dbSNP: rs17310467
rs17310467
Entrez Id: 2937;57644
Gene Symbol: GSS;MYH7B
GSS;MYH7B
CUI: C0919677
Disease:
Protein C measurement 		0.800 GeneticVariation GWASCAT Genome wide association study for plasma levels of natural anticoagulant inhibitors and protein C anticoagulant pathway: the MARTHA project. 22443383 2012
dbSNP: rs17310467
rs17310467
Entrez Id: 2937;57644
Gene Symbol: GSS;MYH7B
GSS;MYH7B
CUI: C1168438
Disease:
Protein C antigen measurement 		0.800 GeneticVariation GWASDB Genome wide association study for plasma levels of natural anticoagulant inhibitors and protein C anticoagulant pathway: the MARTHA project. 22443383 2012
dbSNP: rs11906160
rs11906160
Entrez Id: 57644
Gene Symbol: MYH7B
MYH7B
CUI: C1168438
Disease:
Protein C antigen measurement 		0.800 GeneticVariation GWASCAT A genome-wide association study of the Protein C anticoagulant pathway. 22216198 2011
dbSNP: rs11906160
rs11906160
Entrez Id: 57644
Gene Symbol: MYH7B
MYH7B
CUI: C0919677
Disease:
Protein C measurement 		0.800 GeneticVariation GWASDB A genome-wide association study of the Protein C anticoagulant pathway. 22216198 2011
dbSNP: rs11906160
rs11906160
Entrez Id: 57644
Gene Symbol: MYH7B
MYH7B
CUI: C0919677
Disease:
Protein C measurement 		0.800 GeneticVariation GWASCAT A genome-wide association study of the Protein C anticoagulant pathway. 22216198 2011
dbSNP: rs11906160
rs11906160
Entrez Id: 57644
Gene Symbol: MYH7B
MYH7B
CUI: C1168438
Disease:
Protein C antigen measurement 		0.800 GeneticVariation GWASDB A genome-wide association study of the Protein C anticoagulant pathway. 22216198 2011
dbSNP: rs11906160
rs11906160
Entrez Id: 57644
Gene Symbol: MYH7B
MYH7B
CUI: C0919677
Disease:
Protein C measurement 		0.800 GeneticVariation GWASDB Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study. 20802025 2010
dbSNP: rs11906160
rs11906160
Entrez Id: 57644
Gene Symbol: MYH7B
MYH7B
CUI: C1168438
Disease:
Protein C antigen measurement 		0.800 GeneticVariation GWASDB Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study. 20802025 2010
dbSNP: rs17310467
rs17310467
Entrez Id: 2937;57644
Gene Symbol: GSS;MYH7B
GSS;MYH7B
CUI: C0919677
Disease:
Protein C measurement 		0.800 GeneticVariation GWASDB Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study. 20802025 2010
dbSNP: rs17310467
rs17310467
Entrez Id: 2937;57644
Gene Symbol: GSS;MYH7B
GSS;MYH7B
CUI: C1168438
Disease:
Protein C antigen measurement 		0.800 GeneticVariation GWASDB Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study. 20802025 2010
dbSNP: rs1885120
rs1885120
Entrez Id: 57644;574501;107985393
Gene Symbol: MYH7B;MIR499A;LOC107985393
MYH7B;MIR499A;LOC107985393
CUI: C0025202
Disease:
melanoma 		0.800 GeneticVariation GWASDB Using pooling, we identified a new melanoma risk locus on chromosome 20 (rs910873 and rs1885120), with replication in two further samples (combined P < 1 x 10(-15)). 18488026 2008
dbSNP: rs3746448
rs3746448
Entrez Id: 57644
Gene Symbol: MYH7B
MYH7B
CUI: C0005612
Disease:
Birth Weight 		C 0.700 GeneticVariation GWASCAT Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors. 31043758 2019
dbSNP: rs6060139
rs6060139
Entrez Id: 57644
Gene Symbol: MYH7B
MYH7B
CUI: C0201976
Disease:
Creatinine measurement, serum (procedure) 		C 0.700 GeneticVariation GWASCAT Sex-specific and pleiotropic effects underlying kidney function identified from GWAS meta-analysis. 31015462 2019
dbSNP: rs1885120
rs1885120
Entrez Id: 57644;574501;107985393
Gene Symbol: MYH7B;MIR499A;LOC107985393
MYH7B;MIR499A;LOC107985393
CUI: C0406208
Disease:
Suntan 		C 0.700 GeneticVariation GWASCAT Genome-wide association study in 176,678 Europeans reveals genetic loci for tanning response to sun exposure. 29739929 2018
dbSNP: rs3746446
rs3746446
Entrez Id: 57644
Gene Symbol: MYH7B
MYH7B
CUI: C4551854
Disease:
HYPOPLASTIC LEFT HEART SYNDROME 1 		G 0.700 GeneticVariation GWASCAT A genome-wide association study of congenital cardiovascular left-sided lesions shows association with a locus on chromosome 20. 26965164 2016
dbSNP: rs3746446
rs3746446
Entrez Id: 57644
Gene Symbol: MYH7B
MYH7B
CUI: C3280795
Disease:
HYPOPLASTIC LEFT HEART SYNDROME 2 		G 0.700 GeneticVariation GWASCAT A genome-wide association study of congenital cardiovascular left-sided lesions shows association with a locus on chromosome 20. 26965164 2016
dbSNP: rs2425012
rs2425012
Entrez Id: 57644
Gene Symbol: MYH7B
MYH7B
CUI: C0489786
Disease:
Height 		0.700 GeneticVariation GWASDB Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height. 21194676 2011
dbSNP: rs1058003
rs1058003
Entrez Id: 26133;57644
Gene Symbol: TRPC4AP;MYH7B
TRPC4AP;MYH7B
CUI: C1168438
Disease:
Protein C antigen measurement 		0.700 GeneticVariation GWASDB Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study. 20802025 2010
dbSNP: rs1058003
rs1058003
Entrez Id: 26133;57644
Gene Symbol: TRPC4AP;MYH7B
TRPC4AP;MYH7B
CUI: C0919677
Disease:
Protein C measurement 		0.700 GeneticVariation GWASDB Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study. 20802025 2010
dbSNP: rs13041792
rs13041792
Entrez Id: 2937;57644
Gene Symbol: GSS;MYH7B
GSS;MYH7B
CUI: C1168438
Disease:
Protein C antigen measurement 		0.700 GeneticVariation GWASDB Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study. 20802025 2010
dbSNP: rs13041792
rs13041792
Entrez Id: 2937;57644
Gene Symbol: GSS;MYH7B
GSS;MYH7B
CUI: C0919677
Disease:
Protein C measurement 		0.700 GeneticVariation GWASDB Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study. 20802025 2010
dbSNP: rs17401737
rs17401737
Entrez Id: 57644
Gene Symbol: MYH7B
MYH7B
CUI: C1168438
Disease:
Protein C antigen measurement 		0.700 GeneticVariation GWASDB Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study. 20802025 2010