PRMT7, protein arginine methyltransferase 7, 54496

N. diseases: 65; N. variants: 13
Disease: Skeletal dysplasia ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1251713297
rs1251713297
Entrez Id: 54496
Gene Symbol: PRMT7
PRMT7
CUI: C0410528
Disease:
Skeletal dysplasia 		A 0.700 CausalMutation CLINVAR