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rs35897051

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs35897051(A;C)
Make rs35897051(C;C)
ReferenceGRCh38 38.1/142
Chromosome17
Position58270865
GeneMPO
is asnp
is mentioned by
dbSNPrs35897051
ebirs35897051
HLIrs35897051
Exacrs35897051
Varsomers35897051
Maprs35897051
PheGenIrs35897051
hapmaprs35897051
1000 genomesrs35897051
hgdprs35897051
ensemblrs35897051
gopubmedrs35897051
geneviewrs35897051
scholarrs35897051
googlers35897051
pharmgkbrs35897051
gwascentralrs35897051
openSNPrs35897051
23andMers35897051
23andMe allrs35897051
SNP Nexus

SNPshotrs35897051
SNPdbers35897051
MSV3drs35897051
GWAS Ctlgrs35897051
GMAF0.001377
Max Magnitude0

[PMID 23620142OA-icon.png] Genome-wide and Gene-Centric Analyses of Circulating Myeloperoxidase Levels in the CHARGE and CARe Consortia

ClinVar
Risk rs35897051(C;C)
Alt rs35897051(C;C)
Reference rs35897051(A;A)
Significance Pathogenic
Disease Myeloperoxidase deficiency
Variation info
Gene MPO
CLNDBN Myeloperoxidase deficiency
Reversed 1
HGVS NC_000017.10:g.56348226T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000003816.5,