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rs2234921

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs2234921(A;G)
Make rs2234921(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome22
Position32801088
GeneSYN3, TIMP3
is asnp
is mentioned by
dbSNPrs2234921
dbSNP (old)rs2234921
ClinGenrs2234921
ebirs2234921
HLIrs2234921
Exacrs2234921
Gnomadrs2234921
Varsomers2234921
Maprs2234921
PheGenIrs2234921
Biobankrs2234921
1000 genomesrs2234921
hgdprs2234921
ensemblrs2234921
gopubmedrs2234921
geneviewrs2234921
scholarrs2234921
googlers2234921
pharmgkbrs2234921
gwascentralrs2234921
openSNPrs2234921
23andMers2234921
23andMe allrs2234921
SNP Nexus

SNPshotrs2234921
SNPdbers2234921
MSV3drs2234921
GWAS Ctlgrs2234921
Max Magnitude0

[PMID 25128867] Association of tissue inhibitor of metalloproteinase gene polymorphisms and unexplained recurrent spontaneous abortions in Han Chinese couples


ClinVar
Risk rs2234921(G;G)
Alt rs2234921(G;G)
Reference Rs2234921(A;A)
Significance Non-pathogenic
Disease Pseudoinflammatory fundus dystrophy
Variation info
Gene SYN3 TIMP3
CLNDBN Pseudoinflammatory fundus dystrophy
Reversed 0
HGVS NC_000022.10:g.33197074A>G
CLNSRC
CLNACC RCV000345010.1,