Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs770214071
rs770214071
AAAS
CUI: C0271742
Disease: Glucocorticoid deficiency with achalasia
Glucocorticoid deficiency with achalasia 		T 0.700 CausalMutation CLINVAR AAA syndrome--adrenal insufficiency, alacrima and achalasia. 21865313

2012
dbSNP: rs770214071
rs770214071
AAAS
CUI: C0271742
Disease: Glucocorticoid deficiency with achalasia
Glucocorticoid deficiency with achalasia 		T 0.700 GeneticVariation CLINVAR AAA syndrome--adrenal insufficiency, alacrima and achalasia. 21865313

2012
dbSNP: rs770214071
rs770214071
AAAS
CUI: C0271742
Disease: Glucocorticoid deficiency with achalasia
Glucocorticoid deficiency with achalasia 		T 0.700 CausalMutation CLINVAR Clinical and genetic characterization of families with triple A (Allgrove) syndrome. 12429595

2002
dbSNP: rs770214071
rs770214071
AAAS
CUI: C0271742
Disease: Glucocorticoid deficiency with achalasia
Glucocorticoid deficiency with achalasia 		T 0.700 GeneticVariation CLINVAR Clinical and genetic characterization of families with triple A (Allgrove) syndrome. 12429595

2002