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rs1476413

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common/normal
Make rs1476413(A;A)
Make rs1476413(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position11792243
GeneMTHFR
is asnp
is mentioned by
dbSNPrs1476413
dbSNP (classic)rs1476413
ClinGenrs1476413
ebirs1476413
HLIrs1476413
Exacrs1476413
Gnomadrs1476413
Varsomers1476413
LitVarrs1476413
Maprs1476413
PheGenIrs1476413
Biobankrs1476413
1000 genomesrs1476413
hgdprs1476413
ensemblrs1476413
geneviewrs1476413
scholarrs1476413
googlers1476413
pharmgkbrs1476413
gwascentralrs1476413
openSNPrs1476413
23andMers1476413
SNPshotrs1476413
SNPdbers1476413
MSV3drs1476413
GWAS Ctlgrs1476413
GMAF0.2176
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 19593234OA-icon.png] Association analyses suggest multiple interaction effects of the methylenetetrahydrofolate reductase polymorphisms on timing of menarche and natural menopause in white women


[PMID 22241680OA-icon.png] Deep sequencing study of the MTHFR gene to identify variants associated with myelomeningocele


[PMID 22747749OA-icon.png] Genetic variation in Glutathione S-Transferase Omega-1, Arsenic Methyltransferase and Methylene-tetrahydrofolate Reductase, arsenic exposure and bladder cancer: a case-control study


[PMID 19048631OA-icon.png] Oral facial clefts and gene polymorphisms in metabolism of folate/one-carbon and vitamin A: a pathway-wide association study.


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


[PMID 20962791] Methylenetetrahydrofolate reductase gene polymorphisms and cerebral palsy in Chinese infants.


[PMID 23893618] Association of dietary and supplemental folate intake and polymorphisms in three FOCM pathway genes with colorectal cancer in a population-based case-control study


[PMID 22903727OA-icon.png] Maternal and infant gene-folate interactions and the risk of neural tube defects.