rs1057518391

Orientation

minus

Stabilized

minus

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

Make rs1057518391(A;C)

Make rs1057518391(C;C)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

102948052

Gene

MMP13

is a	snp
is	mentioned by
dbSNP	rs1057518391
dbSNP (classic)	rs1057518391
ClinGen	rs1057518391
ebi	rs1057518391
HLI	rs1057518391
Exac	rs1057518391
Gnomad	rs1057518391
Varsome	rs1057518391
LitVar	rs1057518391
Map	rs1057518391
PheGenI	rs1057518391
Biobank	rs1057518391
1000 genomes	rs1057518391
hgdp	rs1057518391
ensembl	rs1057518391
geneview	rs1057518391
scholar	rs1057518391
google	rs1057518391
pharmgkb	rs1057518391
gwascentral	rs1057518391
openSNP	rs1057518391
23andMe	rs1057518391
SNPshot	rs1057518391
SNPdbe	rs1057518391
MSV3d	rs1057518391
GWAS Ctlg	rs1057518391

Max Magnitude

0

ClinVar
Risk	rs1057518391(C;C)
Alt	rs1057518391(C;C)
Reference	Rs1057518391(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MMP13
CLNDBN	not provided
Reversed	1
HGVS	NC_000011.9:g.102818781T>G
CLNSRC
CLNACC	RCV000414263.1,