TIMP2, TIMP metallopeptidase inhibitor 2, 7077

N. diseases: 404; N. variants: 20
Disease: Androgen-Insensitivity Syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs8179090
rs8179090
Entrez Id: 7077
Gene Symbol: TIMP2
TIMP2
CUI: C0039585
Disease:
Androgen-Insensitivity Syndrome 		0.010 GeneticVariation BEFREE The single-nucleotide polymorphism SNP-418G/C (rs8179090) in the promoter region of the TIMP-2 gene was not associated with the occurrence of AIS. 21228746 2012