rs8179090

minus

Geno	Mag	Summary
(G;G)	0	common in complete genomics

Make rs8179090(C;C)

Make rs8179090(C;G)

Reference

GRCh38 38.1/141

Chromosome

17

Position

78925807

Gene

TIMP2

is a	snp
is	mentioned by
dbSNP	rs8179090
dbSNP (classic)	rs8179090
ClinGen	rs8179090
ebi	rs8179090
HLI	rs8179090
Exac	rs8179090
Gnomad	rs8179090
Varsome	rs8179090
LitVar	rs8179090
Map	rs8179090
PheGenI	rs8179090
Biobank	rs8179090
1000 genomes	rs8179090
hgdp	rs8179090
ensembl	rs8179090
geneview	rs8179090
scholar	rs8179090
google	rs8179090
pharmgkb	rs8179090
gwascentral	rs8179090
openSNP	rs8179090
23andMe	rs8179090
SNPshot	rs8179090
SNPdbe	rs8179090
MSV3d	rs8179090
GWAS Ctlg	rs8179090

GMAF

0.04867

Max Magnitude

0

[PMID 22621753] Higher risk of matrix metalloproteinase (MMP-2, 7, 9) and tissue inhibitor of metalloproteinase (TIMP-2) genetic variants to gallbladder cancer[PMID 19431211 ] Polymorphisms in tissue inhibitors of metalloproteinases-2 and -3 and breast cancer susceptibility and survival.

[PMID 21228746] A promoter polymorphism of tissue inhibitor of metalloproteinase-2 gene is associated with severity of thoracic adolescent idiopathic scoliosis. [PMID 23038618] A replication study for association of 5 single nucleotide polymorphisms with curve progression of adolescent idiopathic scoliosis in Japanese patients.

[PMID 31826071] Interleukin 28 Polymorphisms and Hepatocellular Carcinoma Development after Direct Acting Antiviral Therapy for Chronic Hepatitis C.