Rs121434297

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Orientationminus
is asnp
is mentioned by
dbSNPrs121434297
PheGenIrs121434297
nextbiors121434297
hapmaprs121434297
1000 genomesrs121434297
hgdprs121434297
ensemblrs121434297
gopubmedrs121434297
geneviewrs121434297
scholarrs121434297
googlers121434297
pharmgkbrs121434297
gwascentralrs121434297
openSNPrs121434297
23andMers121434297
23andMe allrs121434297
SNP Nexus

SNPshotrs121434297
SNPdbers121434297
MSV3drs121434297
GeneMTHFR
Chromosome1
Orientationminus
Position11855218
ReferenceGRCh37 37.1/132
Max Magnitude0
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121434297(C;C)
Make rs121434297(C;T)
OMIM607093
Desc
Variant0012
Relatedalso
ClinVar
Risk rs121434297(C;C)
Alt rs121434297(C;C)
Reference rs121434297(T;T)
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.11855218A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000003707.1