rs786205497

Orientation

plus

Stabilized

plus

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

Make rs786205497(A;A)

Make rs786205497(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

55485307

Gene

MMP2

is a	snp
is	mentioned by
dbSNP	rs786205497
dbSNP (classic)	rs786205497
ClinGen	rs786205497
ebi	rs786205497
HLI	rs786205497
Exac	rs786205497
Gnomad	rs786205497
Varsome	rs786205497
LitVar	rs786205497
Map	rs786205497
PheGenI	rs786205497
Biobank	rs786205497
1000 genomes	rs786205497
hgdp	rs786205497
ensembl	rs786205497
geneview	rs786205497
scholar	rs786205497
google	rs786205497
pharmgkb	rs786205497
gwascentral	rs786205497
openSNP	rs786205497
23andMe	rs786205497
SNPshot	rs786205497
SNPdbe	rs786205497
MSV3d	rs786205497
GWAS Ctlg	rs786205497

Max Magnitude

0

ClinVar
Risk	rs786205497(A;A)
Alt	rs786205497(A;A)
Reference	Rs786205497(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MMP2
CLNDBN	not provided
Reversed	0
HGVS	NC_000016.9:g.55519219G>A
CLNSRC
CLNACC	RCV000171246.1,