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rs11547635

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs11547635(C;T)
Make rs11547635(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome22
Position32857305
GeneSYN3, TIMP3
is asnp
is mentioned by
dbSNPrs11547635
dbSNP (old)rs11547635
ClinGenrs11547635
ebirs11547635
HLIrs11547635
Exacrs11547635
Varsomers11547635
Maprs11547635
PheGenIrs11547635
Biobankrs11547635
1000 genomesrs11547635
hgdprs11547635
ensemblrs11547635
gopubmedrs11547635
geneviewrs11547635
scholarrs11547635
googlers11547635
pharmgkbrs11547635
gwascentralrs11547635
openSNPrs11547635
23andMers11547635
23andMe allrs11547635
SNP Nexus

SNPshotrs11547635
SNPdbers11547635
MSV3drs11547635
GWAS Ctlgrs11547635
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 26579821OA-icon.png] Polymorphisms and Plasma Levels of Tissue Inhibitor of Metalloproteinase-3: Impact on Genetic Susceptibility and Clinical Outcome of Oral Cancer


ClinVar
Risk rs11547635(T;T)
Alt rs11547635(T;T)
Reference Rs11547635(C;C)
Significance Non-pathogenic
Disease Pseudoinflammatory fundus dystrophy
Variation info
Gene SYN3 TIMP3
CLNDBN Pseudoinflammatory fundus dystrophy
Reversed 0
HGVS NC_000022.10:g.33253292C>T
CLNSRC
CLNACC RCV000270768.1,