Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs374016704
rs374016704
Entrez Id: 2657;5976;10715
Gene Symbol: GDF1;UPF1;CERS1
GDF1;UPF1;CERS1
CUI: C3178805
Disease:
Heterotaxy Syndrome
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
Entrez Id: 2657;5976;10715
Gene Symbol: GDF1;UPF1;CERS1
GDF1;UPF1;CERS1
CUI: C3178805
Disease:
Heterotaxy Syndrome
G 0.700 GeneticVariation CLINVAR Clinical application of whole-exome sequencing across clinical indications. 26633542 2016