Gene: NOTCH1 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs864622056
rs864622056
NOTCH1
T 0.700 CausalMutation CLINVAR Haploinsufficiency of the NOTCH1 Receptor as a Cause of Adams-Oliver Syndrome With Variable Cardiac Anomalies. 25963545

2015
dbSNP: rs864622057
rs864622057
NOTCH1
G 0.700 GeneticVariation CLINVAR Haploinsufficiency of the NOTCH1 Receptor as a Cause of Adams-Oliver Syndrome With Variable Cardiac Anomalies. 25963545

2015
dbSNP: rs864622058
rs864622058
NOTCH1
T 0.700 GeneticVariation CLINVAR Haploinsufficiency of the NOTCH1 Receptor as a Cause of Adams-Oliver Syndrome With Variable Cardiac Anomalies. 25963545

2015
dbSNP: rs864622059
rs864622059
NOTCH1
GT 0.700 CausalMutation CLINVAR Haploinsufficiency of the NOTCH1 Receptor as a Cause of Adams-Oliver Syndrome With Variable Cardiac Anomalies. 25963545

2015
dbSNP: rs864622060
rs864622060
NOTCH1
G 0.700 GeneticVariation CLINVAR Haploinsufficiency of the NOTCH1 Receptor as a Cause of Adams-Oliver Syndrome With Variable Cardiac Anomalies. 25963545

2015
dbSNP: rs864622060
rs864622060
NOTCH1
G 0.700 CausalMutation CLINVAR

dbSNP: rs864622061
rs864622061
NOTCH1
CA 0.700 CausalMutation CLINVAR Haploinsufficiency of the NOTCH1 Receptor as a Cause of Adams-Oliver Syndrome With Variable Cardiac Anomalies. 25963545

2015
dbSNP: rs864622063
rs864622063
NOTCH1
T 0.700 CausalMutation CLINVAR Haploinsufficiency of the NOTCH1 Receptor as a Cause of Adams-Oliver Syndrome With Variable Cardiac Anomalies. 25963545

2015