KMT2D, lysine methyltransferase 2D, 8085

N. diseases: 320; N. variants: 266
Disease: Cavernous Sinus Meningioma ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1565779530
rs1565779530
Entrez Id: 8085
Gene Symbol: KMT2D
KMT2D
CUI: C1332865
Disease:
Cavernous Sinus Meningioma 		A 0.700 GeneticVariation CLINVAR