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rs2303080

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs2303080(A;A)
Make rs2303080(A;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position7878311
GeneMTRR
is asnp
is mentioned by
dbSNPrs2303080
dbSNP (classic)rs2303080
ClinGenrs2303080
ebirs2303080
HLIrs2303080
Exacrs2303080
Gnomadrs2303080
Varsomers2303080
LitVarrs2303080
Maprs2303080
PheGenIrs2303080
Biobankrs2303080
1000 genomesrs2303080
hgdprs2303080
ensemblrs2303080
geneviewrs2303080
scholarrs2303080
googlers2303080
pharmgkbrs2303080
gwascentralrs2303080
openSNPrs2303080
23andMers2303080
SNPshotrs2303080
SNPdbers2303080
MSV3drs2303080
GWAS Ctlgrs2303080
GMAF0.04454
Max Magnitude0
? (A;A) (A;T) (T;T) 28


Yasko Methylation Necessary to regenerate Methyl-B12 for use by MTR. Mutation can cause shortage, suggesting a need for more B12.


[PMID 19493349OA-icon.png] 118 SNPs of folate-related genes and risks of spina bifida and conotruncal heart defects.


ClinVar
Risk rs2303080(A;A)
Alt rs2303080(A;A)
Reference Rs2303080(T;T)
Significance Probable-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.7878424T>A
CLNSRC UniProtKB (protein)
CLNACC RCV000126886.2, RCV000266246.1,