ROGDI, rogdi atypical leucine zipper, 79641

N. diseases: 61; N. variants: 12
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1039568775
rs1039568775
Entrez Id: 79641
Gene Symbol: ROGDI
ROGDI
CUI: C0406740
Disease:
Kohlschutter Tonz syndrome 		GC 0.700 CausalMutation CLINVAR
dbSNP: rs1555491350
rs1555491350
Entrez Id: 79641
Gene Symbol: ROGDI
ROGDI
CUI: C0406740
Disease:
Kohlschutter Tonz syndrome 		A 0.700 CausalMutation CLINVAR
dbSNP: rs387907145
rs387907145
Entrez Id: 79641
Gene Symbol: ROGDI
ROGDI
CUI: C4020870
Disease:
Abnormality of the hip joint 		A 0.700 CausalMutation CLINVAR
dbSNP: rs387907145
rs387907145
Entrez Id: 79641
Gene Symbol: ROGDI
ROGDI
CUI: C0575802
Disease:
Small hand 		A 0.700 CausalMutation CLINVAR
dbSNP: rs387907145
rs387907145
Entrez Id: 79641
Gene Symbol: ROGDI
ROGDI
CUI: C1848673
Disease:
Hypoplastic feet 		A 0.700 CausalMutation CLINVAR
dbSNP: rs387907145
rs387907145
Entrez Id: 79641
Gene Symbol: ROGDI
ROGDI
CUI: C4025724
Disease:
Abnormality of the cerebral ventricles 		A 0.700 CausalMutation CLINVAR
dbSNP: rs387907145
rs387907145
Entrez Id: 79641
Gene Symbol: ROGDI
ROGDI
CUI: C4024270
Disease:
Distally placed thumb 		A 0.700 CausalMutation CLINVAR
dbSNP: rs387907145
rs387907145
Entrez Id: 79641
Gene Symbol: ROGDI
ROGDI
CUI: C0431447
Disease:
Synophrys 		A 0.700 CausalMutation CLINVAR
dbSNP: rs387907145
rs387907145
Entrez Id: 79641
Gene Symbol: ROGDI
ROGDI
CUI: C0036439
Disease:
Scoliosis, unspecified 		A 0.700 CausalMutation CLINVAR
dbSNP: rs387907145
rs387907145
Entrez Id: 79641
Gene Symbol: ROGDI
ROGDI
CUI: C1844806
Disease:
Weight less than 3rd percentile 		A 0.700 CausalMutation CLINVAR
dbSNP: rs387907145
rs387907145
Entrez Id: 79641
Gene Symbol: ROGDI
ROGDI
CUI: C0349588
Disease:
Short stature 		A 0.700 CausalMutation CLINVAR
dbSNP: rs387907145
rs387907145
Entrez Id: 79641
Gene Symbol: ROGDI
ROGDI
CUI: C1853487
Disease:
Thick eyebrow 		A 0.700 CausalMutation CLINVAR
dbSNP: rs387907145
rs387907145
Entrez Id: 79641
Gene Symbol: ROGDI
ROGDI
CUI: C4021739
Disease:
Abnormality of the acetabulum 		A 0.700 CausalMutation CLINVAR
dbSNP: rs387907145
rs387907145
Entrez Id: 79641
Gene Symbol: ROGDI
ROGDI
CUI: C4025165
Disease:
Cutaneous syndactyly between fingers 2 and 5 		A 0.700 CausalMutation CLINVAR
dbSNP: rs387907145
rs387907145
Entrez Id: 79641
Gene Symbol: ROGDI
ROGDI
CUI: C1849340
Disease:
Long palpebral fissure 		A 0.700 CausalMutation CLINVAR
dbSNP: rs387907145
rs387907145
Entrez Id: 79641
Gene Symbol: ROGDI
ROGDI
CUI: C4020847
Disease:
Abnormality of pelvic girdle bone morphology 		A 0.700 CausalMutation CLINVAR
dbSNP: rs387907145
rs387907145
Entrez Id: 79641
Gene Symbol: ROGDI
ROGDI
CUI: C0406740
Disease:
Kohlschutter Tonz syndrome 		A 0.700 CausalMutation CLINVAR
dbSNP: rs387907145
rs387907145
Entrez Id: 79641
Gene Symbol: ROGDI
ROGDI
CUI: C0036572
Disease:
Seizures 		A 0.700 CausalMutation CLINVAR
dbSNP: rs387907145
rs387907145
Entrez Id: 79641
Gene Symbol: ROGDI
ROGDI
CUI: C0344482
Disease:
Hypoplasia of corpus callosum 		A 0.700 CausalMutation CLINVAR
dbSNP: rs387907145
rs387907145
Entrez Id: 79641
Gene Symbol: ROGDI
ROGDI
CUI: C1861324
Disease:
Short philtrum 		A 0.700 CausalMutation CLINVAR
dbSNP: rs387907145
rs387907145
Entrez Id: 79641
Gene Symbol: ROGDI
ROGDI
CUI: C1845847
Disease:
Coarse facial features 		A 0.700 CausalMutation CLINVAR
dbSNP: rs387907145
rs387907145
Entrez Id: 79641
Gene Symbol: ROGDI
ROGDI
CUI: C0026838
Disease:
Muscle Spasticity 		A 0.700 CausalMutation CLINVAR
dbSNP: rs387907145
rs387907145
Entrez Id: 79641
Gene Symbol: ROGDI
ROGDI
CUI: C1836543
Disease:
Thick vermilion border 		A 0.700 CausalMutation CLINVAR
dbSNP: rs387907145
rs387907145
Entrez Id: 79641
Gene Symbol: ROGDI
ROGDI
CUI: C0333068
Disease:
Flexion contracture 		A 0.700 CausalMutation CLINVAR
dbSNP: rs387907145
rs387907145
Entrez Id: 79641
Gene Symbol: ROGDI
ROGDI
CUI: C4025701
Disease:
Abnormality of the cerebral cortex 		A 0.700 CausalMutation CLINVAR