PRMT7, protein arginine methyltransferase 7, 54496

N. diseases: 65; N. variants: 13
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: C0021655
Disease:
Insulin Resistance
A 0.700 CausalMutation CLINVAR
dbSNP: rs1251713297
rs1251713297
Entrez Id: 54496
Gene Symbol: PRMT7
PRMT7
CUI: C0085271
Disease:
Self-Injurious Behavior
A 0.700 CausalMutation CLINVAR
dbSNP: rs1251713297
rs1251713297
Entrez Id: 54496
Gene Symbol: PRMT7
PRMT7
CUI: C1837084
Disease:
Short metacarpal
A 0.700 CausalMutation CLINVAR
dbSNP: rs1251713297
rs1251713297
Entrez Id: 54496
Gene Symbol: PRMT7
PRMT7
CUI: C0262444
Disease:
Abnormality of the dentition
A 0.700 CausalMutation CLINVAR
dbSNP: rs1251713297
rs1251713297
Entrez Id: 54496
Gene Symbol: PRMT7
PRMT7
CUI: C0428465
Disease:
Serum lipids high (finding)
A 0.700 CausalMutation CLINVAR
dbSNP: rs1251713297
rs1251713297
Entrez Id: 54496
Gene Symbol: PRMT7
PRMT7
CUI: C0424503
Disease:
Dysmorphic facies
A 0.700 CausalMutation CLINVAR
dbSNP: rs1251713297
rs1251713297
Entrez Id: 54496
Gene Symbol: PRMT7
PRMT7
CUI: C1184923
Disease:
Lumbar hyperlordosis
A 0.700 CausalMutation CLINVAR
dbSNP: rs1251713297
rs1251713297
Entrez Id: 54496
Gene Symbol: PRMT7
PRMT7
CUI: C0349588
Disease:
Short stature
A 0.700 CausalMutation CLINVAR
dbSNP: rs1251713297
rs1251713297
Entrez Id: 54496
Gene Symbol: PRMT7
PRMT7
CUI: C0266295
Disease:
Congenital hypoplasia of kidney
A 0.700 CausalMutation CLINVAR
dbSNP: rs1251713297
rs1251713297
Entrez Id: 54496
Gene Symbol: PRMT7
PRMT7
CUI: C2711227
Disease:
Steatohepatitis
A 0.700 CausalMutation CLINVAR
dbSNP: rs1251713297
rs1251713297
Entrez Id: 54496
Gene Symbol: PRMT7
PRMT7
CUI: C0000889
Disease:
Acanthosis Nigricans
A 0.700 CausalMutation CLINVAR
dbSNP: rs1251713297
rs1251713297
Entrez Id: 54496
Gene Symbol: PRMT7
PRMT7
CUI: C0036857
Disease:
Severe intellectual disability
A 0.700 CausalMutation CLINVAR
dbSNP: rs1251713297
rs1251713297
Entrez Id: 54496
Gene Symbol: PRMT7
PRMT7
CUI: C0410528
Disease:
Skeletal dysplasia
A 0.700 CausalMutation CLINVAR
dbSNP: rs1251713297
rs1251713297
Entrez Id: 54496
Gene Symbol: PRMT7
PRMT7
CUI: C0221357
Disease:
Brachydactyly
A 0.700 CausalMutation CLINVAR
dbSNP: rs1567690011
rs1567690011
Entrez Id: 54496
Gene Symbol: PRMT7
PRMT7
CUI: C4021535
Disease:
Infantile sensorineural hearing impairment
C 0.700 CausalMutation CLINVAR
dbSNP: rs1567690011
rs1567690011
Entrez Id: 54496
Gene Symbol: PRMT7
PRMT7
CUI: C0557874
Disease:
Global developmental delay
C 0.700 CausalMutation CLINVAR
dbSNP: rs1567690011
rs1567690011
Entrez Id: 54496
Gene Symbol: PRMT7
PRMT7
CUI: C0221357
Disease:
Brachydactyly
C 0.700 CausalMutation CLINVAR
dbSNP: rs1567690011
rs1567690011
Entrez Id: 54496
Gene Symbol: PRMT7
PRMT7
CUI: C1860816
Disease:
Preauricular skin tag
C 0.700 CausalMutation CLINVAR
dbSNP: rs1567690011
rs1567690011
Entrez Id: 54496
Gene Symbol: PRMT7
PRMT7
CUI: C1386048
Disease:
Intrauterine retardation
C 0.700 CausalMutation CLINVAR
dbSNP: rs1567690011
rs1567690011
Entrez Id: 54496
Gene Symbol: PRMT7
PRMT7
CUI: C0020224
Disease:
Polyhydramnios
C 0.700 CausalMutation CLINVAR
dbSNP: rs1567690011
rs1567690011
Entrez Id: 54496
Gene Symbol: PRMT7
PRMT7
CUI: C0423224
Disease:
Sunken eyes
C 0.700 CausalMutation CLINVAR
dbSNP: rs1567690011
rs1567690011
Entrez Id: 54496
Gene Symbol: PRMT7
PRMT7
CUI: C3806604
Disease:
Infantile axial hypotonia
C 0.700 CausalMutation CLINVAR
dbSNP: rs1567690011
rs1567690011
Entrez Id: 54496
Gene Symbol: PRMT7
PRMT7
CUI: C4310689
Disease:
SHORT STATURE, BRACHYDACTYLY, INTELLECTUAL DEVELOPMENTAL DISABILITY, AND SEIZURES
C 0.700 CausalMutation CLINVAR
dbSNP: rs1567721991
rs1567721991
Entrez Id: 54496
Gene Symbol: PRMT7
PRMT7
CUI: C1386048
Disease:
Intrauterine retardation
TGCTCTCCG 0.700 CausalMutation CLINVAR
dbSNP: rs1567721991
rs1567721991
Entrez Id: 54496
Gene Symbol: PRMT7
PRMT7
CUI: C0557874
Disease:
Global developmental delay
TGCTCTCCG 0.700 CausalMutation CLINVAR