PRMT7, protein arginine methyltransferase 7, 54496

N. diseases: 65; N. variants: 13
Disease: Intrauterine retardation ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1567690011
rs1567690011 		0.882 0.080 16 68337496 frameshift variant AG/- delins
CUI: C1386048
Disease: Intrauterine retardation
Intrauterine retardation 		0.700 0
dbSNP: rs1567721991
rs1567721991 		0.882 0.080 16 68347257 frameshift variant -/GCTCTCCG delins
CUI: C1386048
Disease: Intrauterine retardation
Intrauterine retardation 		0.700 0