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: rs7546
rs7546
Entrez Id: 79641
Gene Symbol: ROGDI
ROGDI
CUI: C0006826
Disease:
Malignant Neoplasms
C 0.700 GeneticVariation GWASCAT Cancer risk susceptibility loci in a Swedish population. 29299148 2017
dbSNP: rs570952151
rs570952151
Entrez Id: 79641
Gene Symbol: ROGDI
ROGDI
CUI: C0406740
Disease:
Kohlschutter Tonz syndrome
T 0.700 CausalMutation CLINVAR Kohlschütter-Tönz syndrome: mutations in ROGDI and evidence of genetic heterogeneity. 23086778 2013
dbSNP: rs1060502981
rs1060502981
Entrez Id: 79641
Gene Symbol: ROGDI
ROGDI
CUI: C0406740
Disease:
Kohlschutter Tonz syndrome
C 0.700 GeneticVariation CLINVAR Mutations in ROGDI Cause Kohlschütter-Tönz Syndrome. 22424600 2012
dbSNP: rs570952151
rs570952151
Entrez Id: 79641
Gene Symbol: ROGDI
ROGDI
CUI: C0406740
Disease:
Kohlschutter Tonz syndrome
T 0.700 CausalMutation CLINVAR Mutations in ROGDI Cause Kohlschütter-Tönz Syndrome. 22424600 2012
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