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rs17466684

From SNPedia

Orientationplus
Stabilizedplus
Make rs17466684(A;A)
Make rs17466684(A;G)
Make rs17466684(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position27595330
GeneEPHX2
is asnp
is mentioned by
dbSNPrs17466684
dbSNP (classic)rs17466684
ClinGenrs17466684
ebirs17466684
HLIrs17466684
Exacrs17466684
Gnomadrs17466684
Varsomers17466684
LitVarrs17466684
Maprs17466684
PheGenIrs17466684
Biobankrs17466684
1000 genomesrs17466684
hgdprs17466684
ensemblrs17466684
geneviewrs17466684
scholarrs17466684
googlers17466684
pharmgkbrs17466684
gwascentralrs17466684
openSNPrs17466684
23andMers17466684
SNPshotrs17466684
SNPdbers17466684
MSV3drs17466684
GWAS Ctlgrs17466684
GMAF0.14
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 19165232]
Trait Panic disorder
Title Genome-wide association study of panic disorder in the Japanese population
Risk Allele
P-val 7E-7
Odds Ratio NR NR



[PMID 18806885OA-icon.png] Genetic analysis of the clusterin gene in pseudoexfoliation syndrome.


[PMID 22234156OA-icon.png] Association of TCF4 and CLU polymorphisms with Fuchs' endothelial dystrophy and implication of CLU and TGFBI proteins in the disease process.



[PMID 26550359OA-icon.png] Association between clusterin polymorphisms and esophageal squamous cell carcinoma risk in Han Chinese population