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rs119469012

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs119469012(G;G)
Make rs119469012(G;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position58272825
GeneMPO
is asnp
is mentioned by
dbSNPrs119469012
ebirs119469012
HLIrs119469012
Exacrs119469012
Varsomers119469012
Maprs119469012
PheGenIrs119469012
hapmaprs119469012
1000 genomesrs119469012
hgdprs119469012
ensemblrs119469012
gopubmedrs119469012
geneviewrs119469012
scholarrs119469012
googlers119469012
pharmgkbrs119469012
gwascentralrs119469012
openSNPrs119469012
23andMers119469012
23andMe allrs119469012
SNP Nexus

SNPshotrs119469012
SNPdbers119469012
MSV3drs119469012
GWAS Ctlgrs119469012
Max Magnitude0
OMIM606989
Desc
Variant0006
Relatedalso
ClinVar
Risk rs119469012(G;G)
Alt rs119469012(G;G)
Reference rs119469012(T;T)
Significance Pathogenic
Disease Myeloperoxidase deficiency
Variation info
Gene MPO
CLNDBN Myeloperoxidase deficiency
Reversed 1
HGVS NC_000017.10:g.56350186A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000003815.3,