Rs121434296

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Orientationminus
is asnp
is mentioned by
dbSNPrs121434296
PheGenIrs121434296
nextbiors121434296
hapmaprs121434296
1000 genomesrs121434296
hgdprs121434296
ensemblrs121434296
gopubmedrs121434296
geneviewrs121434296
scholarrs121434296
googlers121434296
pharmgkbrs121434296
gwascentralrs121434296
openSNPrs121434296
23andMers121434296
23andMe allrs121434296
SNP Nexus

SNPshotrs121434296
SNPdbers121434296
MSV3drs121434296
GeneMTHFR
Chromosome1
Orientationminus
Position11854823
ReferenceGRCh37 37.1/132
Max Magnitude0
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121434296(C;T)
Make rs121434296(T;T)
OMIM607093
Desc
Variant0011
Relatedalso
ClinVar
Risk rs121434296(T;T)
Alt rs121434296(T;T)
Reference rs121434296(C;C)
Significance 5
Disease Homocystinuria due to MTHFR deficiency
ClinVar info
Gene MTHFR
CLNDBN Homocystinuria due to MTHFR deficiency
Reversed 1
CLNHGVS NC_000001.10:g.11854823G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000003706.1