Rs121434295

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Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121434295(A;A)
Make rs121434295(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position11801166
GeneMTHFR
is asnp
is mentioned by
dbSNPrs121434295
PheGenIrs121434295
nextbiors121434295
hapmaprs121434295
1000 genomesrs121434295
hgdprs121434295
ensemblrs121434295
gopubmedrs121434295
geneviewrs121434295
scholarrs121434295
googlers121434295
pharmgkbrs121434295
gwascentralrs121434295
openSNPrs121434295
23andMers121434295
23andMe allrs121434295
SNP Nexus

SNPshotrs121434295
SNPdbers121434295
MSV3drs121434295
Max Magnitude0
OMIM607093
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121434295(A;A)
Alt rs121434295(A;A)
Reference rs121434295(G;G)
Significance Pathogenic
Disease Homocystinuria due to MTHFR deficiency
Variation info
Gene MTHFR
CLNDBN Homocystinuria due to MTHFR deficiency
Reversed 1
HGVS NC_000001.11:g.11801166C>T
CLNSRC ClinVar OMIM Allelic Variant
CLNACC RCV000003696.1,