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rs786205497

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205497(A;A)
Make rs786205497(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position55485307
GeneMMP2
is asnp
is mentioned by
dbSNPrs786205497
ebirs786205497
HLIrs786205497
Exacrs786205497
Varsomers786205497
Maprs786205497
PheGenIrs786205497
hapmaprs786205497
1000 genomesrs786205497
hgdprs786205497
ensemblrs786205497
gopubmedrs786205497
geneviewrs786205497
scholarrs786205497
googlers786205497
pharmgkbrs786205497
gwascentralrs786205497
openSNPrs786205497
23andMers786205497
23andMe allrs786205497
SNP Nexus

SNPshotrs786205497
SNPdbers786205497
MSV3drs786205497
GWAS Ctlgrs786205497
Max Magnitude0
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,