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rs161870

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs161870(C;C)
Make rs161870(C;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position7878079
GeneMTRR
is asnp
is mentioned by
dbSNPrs161870
dbSNP (classic)rs161870
ClinGenrs161870
ebirs161870
HLIrs161870
Exacrs161870
Gnomadrs161870
Varsomers161870
LitVarrs161870
Maprs161870
PheGenIrs161870
Biobankrs161870
1000 genomesrs161870
hgdprs161870
ensemblrs161870
geneviewrs161870
scholarrs161870
googlers161870
pharmgkbrs161870
gwascentralrs161870
openSNPrs161870
23andMers161870
SNPshotrs161870
SNPdbers161870
MSV3drs161870
GWAS Ctlgrs161870
Max Magnitude0

[PMID 23913011OA-icon.png] Role of one-carbon metabolizing pathway genes and gene-nutrient interaction in the risk of non-Hodgkin lymphoma


ClinVar
Risk rs161870(C;C)
Alt rs161870(C;C)
Reference Rs161870(T;T)
Significance Non-pathogenic
Disease not specified Disorders of Intracellular Cobalamin Metabolism
Variation info
Gene MTRR
CLNDBN not specified Disorders of Intracellular Cobalamin Metabolism
Reversed 0
HGVS NC_000005.9:g.7878192T>C
CLNSRC ClinVar GeneDx
CLNACC RCV000126885.2, RCV000307309.1,