Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs374016704
rs374016704
GDF1 ; UPF1 ; CERS1
G 0.700 GeneticVariation CLINVAR Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands. 28991257

2017
dbSNP: rs374016704
rs374016704
GDF1 ; UPF1 ; CERS1
G 0.700 GeneticVariation CLINVAR Clinical application of whole-exome sequencing across clinical indications. 26633542

2016