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rs141055426

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs141055426(A;A)
Make rs141055426(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position58203314
GeneEPX
is asnp
is mentioned by
dbSNPrs141055426
ebirs141055426
HLIrs141055426
Exacrs141055426
Varsomers141055426
Maprs141055426
PheGenIrs141055426
hapmaprs141055426
1000 genomesrs141055426
hgdprs141055426
ensemblrs141055426
gopubmedrs141055426
geneviewrs141055426
scholarrs141055426
googlers141055426
pharmgkbrs141055426
gwascentralrs141055426
openSNPrs141055426
23andMers141055426
23andMe allrs141055426
SNP Nexus

SNPshotrs141055426
SNPdbers141055426
MSV3drs141055426
GWAS Ctlgrs141055426
Max Magnitude0
ClinVar
Risk rs141055426(A;A)
Alt rs141055426(A;A)
Reference rs141055426(G;G)
Significance Other
Disease Eosinophil peroxidase deficiency
Variation info
Gene EPX
CLNDBN Eosinophil peroxidase deficiency
Reversed 0
HGVS NC_000017.10:g.56280675G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000190420.3,