PRMT7, protein arginine methyltransferase 7, 54496

N. diseases: 65; N. variants: 13
Disease: Severe intellectual disability ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1014959895
rs1014959895
Entrez Id: 54496
Gene Symbol: PRMT7
PRMT7
CUI: C0036857
Disease:
Severe intellectual disability 		T 0.700 CausalMutation CLINVAR