Rs121913578

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Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121913578(C;T)
Make rs121913578(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position236895470
GeneMTR
is asnp
is mentioned by
dbSNPrs121913578
PheGenIrs121913578
nextbiors121913578
hapmaprs121913578
1000 genomesrs121913578
hgdprs121913578
ensemblrs121913578
gopubmedrs121913578
geneviewrs121913578
scholarrs121913578
googlers121913578
pharmgkbrs121913578
gwascentralrs121913578
openSNPrs121913578
23andMers121913578
23andMe allrs121913578
SNP Nexus

SNPshotrs121913578
SNPdbers121913578
MSV3drs121913578
Max Magnitude0
OMIM156570
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121913578(T;T)
Alt rs121913578(T;T)
Reference rs121913578(C;C)
Significance Pathogenic
Disease METHYLCOBALAMIN DEFICIENCY
Variation info
Gene MTR
CLNDBN METHYLCOBALAMIN DEFICIENCY, cblG TYPE
Reversed 0
HGVS NC_000001.11:g.236895470C>T
CLNSRC ClinVar OMIM Allelic Variant
CLNACC RCV000015348.25,