MYSM1, Myb like, SWIRM and MPN domains 1, 114803

N. diseases: 37; N. variants: 3
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2811893
rs2811893
Entrez Id: 114803
Gene Symbol: MYSM1
MYSM1
CUI: C0011884
Disease:
Diabetic Retinopathy 		T 0.800 GeneticVariation GWASCAT Genome-wide association study of diabetic retinopathy in a Taiwanese population. 21310492 2011
dbSNP: rs2811893
rs2811893
Entrez Id: 114803
Gene Symbol: MYSM1
MYSM1
CUI: C0011884
Disease:
Diabetic Retinopathy 		T 0.800 GeneticVariation GWASDB Genome-wide association study of diabetic retinopathy in a Taiwanese population. 21310492 2011
dbSNP: rs1557507208
rs1557507208
Entrez Id: 114803
Gene Symbol: MYSM1
MYSM1
CUI: C4748257
Disease:
BONE MARROW FAILURE SYNDROME 4 		C 0.700 CausalMutation CLINVAR
dbSNP: rs1557518298
rs1557518298
Entrez Id: 114803
Gene Symbol: MYSM1
MYSM1
CUI: C4748257
Disease:
BONE MARROW FAILURE SYNDROME 4 		A 0.700 CausalMutation CLINVAR