Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1085307845
rs1085307845
PHIP
CUI: C4022738
Disease: Neurodevelopmental delay
Neurodevelopmental delay 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs1131691771
rs1131691771
PHIP ; IRAK1BP1
CUI: C4022738
Disease: Neurodevelopmental delay
Neurodevelopmental delay 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs1554210073
rs1554210073
PHIP
CUI: C4022738
Disease: Neurodevelopmental delay
Neurodevelopmental delay 		A 0.700 CausalMutation CLINVAR

dbSNP: rs1562114190
rs1562114190
PHIP ; IRAK1BP1
CUI: C4022738
Disease: Neurodevelopmental delay
Neurodevelopmental delay 		G 0.700 CausalMutation CLINVAR

dbSNP: rs1562127631
rs1562127631
PHIP ; IRAK1BP1
CUI: C4022738
Disease: Neurodevelopmental delay
Neurodevelopmental delay 		A 0.700 CausalMutation CLINVAR

dbSNP: rs1562134961
rs1562134961
PHIP ; IRAK1BP1
CUI: C4022738
Disease: Neurodevelopmental delay
Neurodevelopmental delay 		C 0.700 CausalMutation CLINVAR

dbSNP: rs1562150844
rs1562150844
PHIP
CUI: C4022738
Disease: Neurodevelopmental delay
Neurodevelopmental delay 		C 0.700 CausalMutation CLINVAR

dbSNP: rs1562171209
rs1562171209
PHIP
CUI: C4022738
Disease: Neurodevelopmental delay
Neurodevelopmental delay 		C 0.700 GeneticVariation CLINVAR

dbSNP: rs1562203136
rs1562203136
PHIP
CUI: C4022738
Disease: Neurodevelopmental delay
Neurodevelopmental delay 		CT 0.700 CausalMutation CLINVAR

dbSNP: rs755604487
rs755604487
PHIP
CUI: C4022738
Disease: Neurodevelopmental delay
Neurodevelopmental delay 		A 0.700 GeneticVariation CLINVAR