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: C4025701
Disease: Abnormality of the cerebral cortex
Abnormality of the cerebral cortex 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1569355102
rs1569355102
DYRK1A
CUI: C4022561
Disease: Maternal first trimester fever
Maternal first trimester fever 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1569355102
rs1569355102
DYRK1A
CUI: C0349588
Disease: Short stature
Short stature 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1569355102
rs1569355102
DYRK1A
CUI: C0152423
Disease: Congenital small ears
Congenital small ears 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1569355102
rs1569355102
DYRK1A
CUI: C0235942
Disease: Abnormality of the skull
Abnormality of the skull 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1569355102
rs1569355102
DYRK1A
CUI: C0265660
Disease: Syndactyly of the toes
Syndactyly of the toes 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1569355102
rs1569355102
DYRK1A
CUI: C4025790
Disease: Specific learning disability
Specific learning disability 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1569355102
rs1569355102
DYRK1A
CUI: C1854882
Disease: Absent speech
Absent speech 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1569355102
rs1569355102
DYRK1A
CUI: C3532947
Disease: Severe receptive language delay
Severe receptive language delay 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1569355102
rs1569355102
DYRK1A
CUI: C1837142
Disease: Poor suck
Poor suck 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1569355102
rs1569355102
DYRK1A
CUI: C0424503
Disease: Dysmorphic facies
Dysmorphic facies 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1569355102
rs1569355102
DYRK1A
CUI: C4022733
Disease: Widened cerebral subarachnoid space
Widened cerebral subarachnoid space 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1569355102
rs1569355102
DYRK1A
CUI: C0238397
Disease: Pulmonary artery stenosis
Pulmonary artery stenosis 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1569355102
rs1569355102
DYRK1A
CUI: C1848673
Disease: Hypoplastic feet
Hypoplastic feet 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1569355102
rs1569355102
DYRK1A
CUI: C0557874
Disease: Global developmental delay
Global developmental delay 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1569355102
rs1569355102
DYRK1A
CUI: C0235991
Disease: Small for gestational age (disorder)
Small for gestational age (disorder) 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1569355102
rs1569355102
DYRK1A
CUI: C4022765
Disease: Abnormality of the subarachnoid space
Abnormality of the subarachnoid space 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1569355102
rs1569355102
DYRK1A
CUI: C1855650
Disease: Birth length less than 3rd percentile
Birth length less than 3rd percentile 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1569355102
rs1569355102
DYRK1A
CUI: C1860475
Disease: Retinal vascular tortuosity
Retinal vascular tortuosity 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1569355102
rs1569355102
DYRK1A
CUI: C0231255
Disease: Decreased body mass index
Decreased body mass index 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1569355102
rs1569355102
DYRK1A
CUI: C0029131
Disease: Abnormality of the optic nerve
Abnormality of the optic nerve 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1569355102
rs1569355102
DYRK1A
CUI: C3279839
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 7
MENTAL RETARDATION, AUTOSOMAL DOMINANT 7 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1569355102
rs1569355102
DYRK1A
CUI: C0432040
Disease: Simple syndactyly of toes, first web space
Simple syndactyly of toes, first web space 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1569355102
rs1569355102
DYRK1A
CUI: C3532933
Disease: Moderate expressive language delay
Moderate expressive language delay 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1569355102
rs1569355102
DYRK1A
CUI: C2315100
Disease: Pediatric failure to thrive
Pediatric failure to thrive 		T 0.700 CausalMutation CLINVAR