MYH9, myosin heavy chain 9, 4627

N. diseases: 196; N. variants: 38
Disease: Familial hematuria ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11089788
rs11089788
Entrez Id: 4627
Gene Symbol: MYH9
MYH9
CUI: C1305904
Disease:
Familial hematuria 		0.010 GeneticVariation BEFREE Evidence for association with "Severe" progression in CFHR5 nephropathy was found with MYH9 variant rs11089788 and was confirmed in an independent FH cohort, D (cumulative p value = 0.001, odds ratio = 3.06, recessive model). 23516419 2013