rs3819089

Orientation

minus

Stabilized

minus

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

Make rs3819089(A;A)

Make rs3819089(A;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

102952004

Gene

MMP13

is a	snp
is	mentioned by
dbSNP	rs3819089
dbSNP (classic)	rs3819089
ClinGen	rs3819089
ebi	rs3819089
HLI	rs3819089
Exac	rs3819089
Gnomad	rs3819089
Varsome	rs3819089
LitVar	rs3819089
Map	rs3819089
PheGenI	rs3819089
Biobank	rs3819089
1000 genomes	rs3819089
hgdp	rs3819089
ensembl	rs3819089
geneview	rs3819089
scholar	rs3819089
google	rs3819089
pharmgkb	rs3819089
gwascentral	rs3819089
openSNP	rs3819089
23andMe	rs3819089
SNPshot	rs3819089
SNPdbe	rs3819089
MSV3d	rs3819089
GWAS Ctlg	rs3819089

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

[PMID 25100770] Single Nucleotide Polymorphisms in Osteogenic Genes in Atrophic Delayed Fracture-Healing: A Preliminary Investigation

ClinVar
Risk	rs3819089(A;A)
Alt	rs3819089(A;A)
Reference	Rs3819089(G;G)
Significance	Non-pathogenic
Disease	Spondyloepimetaphyseal dysplasia Metaphyseal anadysplasia
Variation	info
Gene	MMP13
CLNDBN	Spondyloepimetaphyseal dysplasia Metaphyseal anadysplasia
Reversed	1
HGVS	NC_000011.9:g.102822733C>T
CLNSRC
CLNACC	RCV000326021.1, RCV000380643.1,