Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1569355102
rs1569355102
DYRK1A
CUI: C1843108
Disease: Short palm
Short palm 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1569355102
rs1569355102
DYRK1A
CUI: C0162834
Disease: Hyperpigmentation
Hyperpigmentation 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1569355102
rs1569355102
DYRK1A
CUI: C1837260
Disease: Prominent forehead
Prominent forehead 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1569355102
rs1569355102
DYRK1A
CUI: C0454641
Disease: Expressive language delay
Expressive language delay 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1569355102
rs1569355102
DYRK1A
CUI: C0151526
Disease: Premature Birth
Premature Birth 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1569355102
rs1569355102
DYRK1A
CUI: C0575802
Disease: Small hand
Small hand 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1569355102
rs1569355102
DYRK1A
CUI: C1855843
Disease: Severe intrauterine growth retardation
Severe intrauterine growth retardation 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1569355102
rs1569355102
DYRK1A
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding) 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1569355102
rs1569355102
DYRK1A
CUI: C0025990
Disease: Micrognathism
Micrognathism 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1569355102
rs1569355102
DYRK1A
CUI: C1867114
Disease: Craniofacial disproportion
Craniofacial disproportion 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1569355102
rs1569355102
DYRK1A
CUI: C1386048
Disease: Intrauterine retardation
Intrauterine retardation 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1569355102
rs1569355102
DYRK1A
CUI: C0454644
Disease: Delayed speech and language development
Delayed speech and language development 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1569355102
rs1569355102
DYRK1A
CUI: C0221263
Disease: Cafe-au-Lait Spots
Cafe-au-Lait Spots 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1569355102
rs1569355102
DYRK1A
CUI: C4021041
Disease: Maternal fever in pregnancy
Maternal fever in pregnancy 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1569355102
rs1569355102
DYRK1A
CUI: C1835884
Disease: Triangular face
Triangular face 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1569355102
rs1569355102
DYRK1A
CUI: C1837503
Disease: Small cerebral cortex
Small cerebral cortex 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1569355102
rs1569355102
DYRK1A
CUI: C4025724
Disease: Abnormality of the cerebral ventricles
Abnormality of the cerebral ventricles 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1569355102
rs1569355102
DYRK1A
CUI: C1861324
Disease: Short philtrum
Short philtrum 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1569355102
rs1569355102
DYRK1A
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1569355102
rs1569355102
DYRK1A
CUI: C4023681
Disease: Delayed fine motor development
Delayed fine motor development 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1569355102
rs1569355102
DYRK1A
CUI: C1844806
Disease: Weight less than 3rd percentile
Weight less than 3rd percentile 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1569355102
rs1569355102
DYRK1A
CUI: C3278923
Disease: Dilated ventricles (finding)
Dilated ventricles (finding) 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1569355102
rs1569355102
DYRK1A
CUI: C1837658
Disease: Gross motor development delay
Gross motor development delay 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1569355102
rs1569355102
DYRK1A
CUI: C0431352
Disease: Secondary microcephaly
Secondary microcephaly 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1569355102
rs1569355102
DYRK1A
CUI: C0454642
Disease: Receptive language delay
Receptive language delay 		T 0.700 CausalMutation CLINVAR