MICALL2, MICAL like 2, 79778

N. diseases: 13; N. variants: 2
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs28403420
rs28403420
Entrez Id: 79778
Gene Symbol: MICALL2
MICALL2
CUI: C0020538
Disease:
Hypertensive disease 		A 0.700 GeneticVariation GWASCAT Genome-Wide Association Study of Apparent Treatment-Resistant Hypertension in the CHARGE Consortium: The CHARGE Pharmacogenetics Working Group. 31545351 2019
dbSNP: rs556808514
rs556808514
Entrez Id: 79778
Gene Symbol: MICALL2
MICALL2
CUI: C4551568
Disease:
Joubert syndrome 1 		C 0.700 CausalMutation CLINVAR