Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6600164
rs6600164
Entrez Id: 23162
Gene Symbol: MAPK8IP3
MAPK8IP3
CUI: C0040420
Disease:
Tonometry 		T 0.700 GeneticVariation GWASCAT Genome-wide association analyses identify new loci influencing intraocular pressure. 29617998 2018
dbSNP: rs770703007
rs770703007
Entrez Id: 23162
Gene Symbol: MAPK8IP3
MAPK8IP3
CUI: C0423082
Disease:
Hypometric saccades 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs770703007
rs770703007
Entrez Id: 23162
Gene Symbol: MAPK8IP3
MAPK8IP3
CUI: C0700078
Disease:
Decreased tendon reflex 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs770703007
rs770703007
Entrez Id: 23162
Gene Symbol: MAPK8IP3
MAPK8IP3
CUI: C0557874
Disease:
Global developmental delay 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs770703007
rs770703007
Entrez Id: 23162
Gene Symbol: MAPK8IP3
MAPK8IP3
CUI: C4023074
Disease:
EEG with parietal focal spikes 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs770703007
rs770703007
Entrez Id: 23162
Gene Symbol: MAPK8IP3
MAPK8IP3
CUI: C2267233
Disease:
Neonatal Hypotonia 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs770703007
rs770703007
Entrez Id: 23162
Gene Symbol: MAPK8IP3
MAPK8IP3
CUI: C4023073
Disease:
EEG with temporal focal spikes 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs770703007
rs770703007
Entrez Id: 23162
Gene Symbol: MAPK8IP3
MAPK8IP3
CUI: C0028738
Disease:
Nystagmus 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs770703007
rs770703007
Entrez Id: 23162
Gene Symbol: MAPK8IP3
MAPK8IP3
CUI: C0013362
Disease:
Dysarthria 		G 0.700 GeneticVariation CLINVAR