Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs775266057
rs775266057
Entrez Id: 5885;84294
Gene Symbol: RAD21;UTP23
RAD21;UTP23
CUI: C1969653
Disease:
MUNGAN SYNDROME
T 0.800 CausalMutation CLINVAR Mutations in RAD21 disrupt regulation of APOB in patients with chronic intestinal pseudo-obstruction. 25575569 2015
dbSNP: rs775266057
rs775266057
Entrez Id: 5885;84294
Gene Symbol: RAD21;UTP23
RAD21;UTP23
CUI: C1969653
Disease:
MUNGAN SYNDROME
0.800 GeneticVariation UNIPROT