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rs1770449

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1770449(A;G)
Make rs1770449(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position236874861
GeneMTR
is asnp
is mentioned by
dbSNPrs1770449
dbSNP (classic)rs1770449
ClinGenrs1770449
ebirs1770449
HLIrs1770449
Exacrs1770449
Gnomadrs1770449
Varsomers1770449
LitVarrs1770449
Maprs1770449
PheGenIrs1770449
Biobankrs1770449
1000 genomesrs1770449
hgdprs1770449
ensemblrs1770449
geneviewrs1770449
scholarrs1770449
googlers1770449
pharmgkbrs1770449
gwascentralrs1770449
openSNPrs1770449
23andMers1770449
SNPshotrs1770449
SNPdbers1770449
MSV3drs1770449
GWAS Ctlgrs1770449
GMAF0.259
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 20180013] Genetic polymorphisms in folate and alcohol metabolism and breast cancer risk: a case-control study in Thai women


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


ClinVar
Risk rs1770449(G;G)
Alt rs1770449(G;G)
Reference Rs1770449(A;A)
Significance Non-pathogenic
Disease not specified Disorders of Intracellular Cobalamin Metabolism
Variation info
Gene MTR
CLNDBN not specified Disorders of Intracellular Cobalamin Metabolism
Reversed 1
HGVS NC_000001.10:g.237038161T>C
CLNSRC ClinVar GeneDx
CLNACC RCV000126867.3, RCV000283784.1,