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rs121434566

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121434566(A;A)
Make rs121434566(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position58196994
GeneEPX
is asnp
is mentioned by
dbSNPrs121434566
ebirs121434566
HLIrs121434566
Exacrs121434566
Varsomers121434566
Maprs121434566
PheGenIrs121434566
hapmaprs121434566
1000 genomesrs121434566
hgdprs121434566
ensemblrs121434566
gopubmedrs121434566
geneviewrs121434566
scholarrs121434566
googlers121434566
pharmgkbrs121434566
gwascentralrs121434566
openSNPrs121434566
23andMers121434566
23andMe allrs121434566
SNP Nexus

SNPshotrs121434566
SNPdbers121434566
MSV3drs121434566
GWAS Ctlgrs121434566
GMAF0.0004591
Max Magnitude0
OMIM131399
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121434566(A;A)
Alt rs121434566(A;A)
Reference rs121434566(G;G)
Significance Other
Disease Eosinophil peroxidase deficiency
Variation info
Gene EPX
CLNDBN Eosinophil peroxidase deficiency
Reversed 0
HGVS NC_000017.10:g.56274355G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000018090.26,