rs2274755

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs2274755(G;T)

Make rs2274755(T;T)

Reference

GRCh38 38.1/141

Chromosome

20

Position

46011053

Gene

MMP9

is a	snp
is	mentioned by
dbSNP	rs2274755
dbSNP (classic)	rs2274755
ClinGen	rs2274755
ebi	rs2274755
HLI	rs2274755
Exac	rs2274755
Gnomad	rs2274755
Varsome	rs2274755
LitVar	rs2274755
Map	rs2274755
PheGenI	rs2274755
Biobank	rs2274755
1000 genomes	rs2274755
hgdp	rs2274755
ensembl	rs2274755
geneview	rs2274755
scholar	rs2274755
google	rs2274755
pharmgkb	rs2274755
gwascentral	rs2274755
openSNP	rs2274755
23andMe	rs2274755
SNPshot	rs2274755
SNPdbe	rs2274755
MSV3d	rs2274755
GWAS Ctlg	rs2274755

GMAF

0.1566

Max Magnitude

0

?

(G;G) (G;T) (T;T)

28

[PMID 23077567 ] Assessment of the association of matrix metalloproteinases with myopia, refractive error and ocular biometric measures in an Australian cohort

[PMID 23639553] Polymorphisms in Metalloproteinase-9 are Associated with the risk for Asthma in Mexican Pediatric Patients

[PMID 20078883 ] Association of MMP-2 polymorphisms with severe and very severe COPD: a case control study of MMPs-1, 9 and 12 in a European population.

[PMID 20181264 ] MMP-9 gene variants increase the risk for non-atopic asthma in children.

[PMID 25162123] MMP9 Gene Polymorphism is not Associated with Polypoidal Choroidal Vasculopathy and Neovascular Age-related Macular Degeneration in a Chinese Han Population

[PMID 27637086 ] A single-nucleotide polymorphism in MMP9 is associated with decreased risk of steroid-induced osteonecrosis of the femoral head.

ClinVar
Risk	rs2274755(T;T)
Alt	rs2274755(T;T)
Reference	Rs2274755(G;G)
Significance	Non-pathogenic
Disease	Metaphyseal anadysplasia
Variation	info
Gene	MMP9
CLNDBN	Metaphyseal anadysplasia
Reversed	0
HGVS	NC_000020.10:g.44639692G>T
CLNSRC
CLNACC	RCV000339225.1,

[PMID 29137306 ] MMP9 polymorphism is associated with susceptibility to non-traumatic osteonecrosis of femoral head in a Chinese Han population.