KMT2A, lysine methyltransferase 2A, 4297

N. diseases: 535; N. variants: 65
Disease: Intrauterine retardation ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555038111
rs1555038111
Entrez Id: 4297
Gene Symbol: KMT2A
KMT2A
CUI: C1386048
Disease:
Intrauterine retardation 		G 0.700 CausalMutation CLINVAR