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rs1076991

From SNPedia

Orientationminus
Stabilizedminus
Make rs1076991(A;A)
Make rs1076991(A;G)
Make rs1076991(G;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position64388323
GeneMTHFD1
is asnp
is mentioned by
dbSNPrs1076991
ebirs1076991
HLIrs1076991
Exacrs1076991
Varsomers1076991
Maprs1076991
PheGenIrs1076991
hapmaprs1076991
1000 genomesrs1076991
hgdprs1076991
ensemblrs1076991
gopubmedrs1076991
geneviewrs1076991
scholarrs1076991
googlers1076991
pharmgkbrs1076991
gwascentralrs1076991
openSNPrs1076991
23andMers1076991
23andMe allrs1076991
SNP Nexus

SNPshotrs1076991
SNPdbers1076991
MSV3drs1076991
GWAS Ctlgrs1076991
GMAF0.4871
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 19130090OA-icon.png] rs1076991 C > T exerts a significant effect on promoter activity in vitro and along with rs2236225 G > A influences embryonic development.


[PMID 19064578OA-icon.png] No association of single nucleotide polymorphisms in one-carbon metabolism genes with prostate cancer risk.


[PMID 19808787OA-icon.png] Genetics of human neural tube defects.


[PMID 23940529OA-icon.png] Roles of genetic polymorphisms in the folate pathway in childhood acute lymphoblastic leukemia evaluated by bayesian relevance and effect size analysis