CHN1, chimerin 1, 1123

N. diseases: 112; N. variants: 13
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1558939623
rs1558939623
Entrez Id: 1123
Gene Symbol: CHN1
CHN1
CUI: C1848873
Disease:
Abnormality of the diaphragm
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1558939623
rs1558939623
Entrez Id: 1123
Gene Symbol: CHN1
CHN1
CUI: C0003706
Disease:
Arachnodactyly
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1558939623
rs1558939623
Entrez Id: 1123
Gene Symbol: CHN1
CHN1
CUI: C1852464
Disease:
Abnormality of the cervical spine
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1558939623
rs1558939623
Entrez Id: 1123
Gene Symbol: CHN1
CHN1
CUI: C0232466
Disease:
Feeding difficulties
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1558939623
rs1558939623
Entrez Id: 1123
Gene Symbol: CHN1
CHN1
CUI: C0025988
Disease:
Microglossia
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1558939623
rs1558939623
Entrez Id: 1123
Gene Symbol: CHN1
CHN1
CUI: C0018784
Disease:
Sensorineural Hearing Loss (disorder)
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1558939623
rs1558939623
Entrez Id: 1123
Gene Symbol: CHN1
CHN1
CUI: C1840379
Disease:
Cerebellar vermis hypoplasia
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1558939623
rs1558939623
Entrez Id: 1123
Gene Symbol: CHN1
CHN1
CUI: C0557874
Disease:
Global developmental delay
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1558939623
rs1558939623
Entrez Id: 1123
Gene Symbol: CHN1
CHN1
CUI: C1846464
Disease:
Globe retraction and deviation on adduction
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1558939623
rs1558939623
Entrez Id: 1123
Gene Symbol: CHN1
CHN1
CUI: C0264303
Disease:
Laryngomalacia
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1558939623
rs1558939623
Entrez Id: 1123
Gene Symbol: CHN1
CHN1
CUI: C0575802
Disease:
Small hand
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1558939623
rs1558939623
Entrez Id: 1123
Gene Symbol: CHN1
CHN1
CUI: C0020295
Disease:
Hydronephrosis
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1558939623
rs1558939623
Entrez Id: 1123
Gene Symbol: CHN1
CHN1
CUI: C0028077
Disease:
Nyctalopia
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1558939623
rs1558939623
Entrez Id: 1123
Gene Symbol: CHN1
CHN1
CUI: C2981150
Disease:
Uranostaphyloschisis
T 0.700 GeneticVariation CLINVAR
dbSNP: rs188245701
rs188245701
Entrez Id: 1123
Gene Symbol: CHN1
CHN1
CUI: C0016529
Disease:
Forced expiratory volume function
T 0.700 GeneticVariation GWASCAT A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry. 26634245 2015
dbSNP: rs387906599
rs387906599
Entrez Id: 1123
Gene Symbol: CHN1
CHN1
CUI: C0751083
Disease:
Duane Retraction Syndrome, Type 2
A 0.700 CausalMutation CLINVAR
dbSNP: rs387906600
rs387906600
Entrez Id: 1123
Gene Symbol: CHN1
CHN1
CUI: C0751083
Disease:
Duane Retraction Syndrome, Type 2
A 0.700 CausalMutation CLINVAR