Disease: EPISODIC PAIN SYNDROME, FAMILIAL, 1 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs398123010
rs398123010
Entrez Id: 8989;100132891
Gene Symbol: TRPA1;MSC-AS1
TRPA1;MSC-AS1
CUI: C3808667
Disease:
EPISODIC PAIN SYNDROME, FAMILIAL, 1 		0.700 GeneticVariation UNIPROT A gain-of-function mutation in TRPA1 causes familial episodic pain syndrome. 20547126 2010