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rs3768160

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs3768160(C;C)
Make rs3768160(C;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position236899132
GeneMTR
is asnp
is mentioned by
dbSNPrs3768160
dbSNP (old)rs3768160
ClinGenrs3768160
ebirs3768160
HLIrs3768160
Exacrs3768160
Gnomadrs3768160
Varsomers3768160
Maprs3768160
PheGenIrs3768160
Biobankrs3768160
1000 genomesrs3768160
hgdprs3768160
ensemblrs3768160
gopubmedrs3768160
geneviewrs3768160
scholarrs3768160
googlers3768160
pharmgkbrs3768160
gwascentralrs3768160
openSNPrs3768160
23andMers3768160
23andMe allrs3768160
SNP Nexus

SNPshotrs3768160
SNPdbers3768160
MSV3drs3768160
GWAS Ctlgrs3768160
GMAF0.08999
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 20737570] Genetic variants in one-carbon metabolism-related genes contribute to NSCLC prognosis in a Chinese population


ClinVar
Risk rs3768160(C;C)
Alt rs3768160(C;C)
Reference Rs3768160(T;T)
Significance Probable-non-pathogenic
Disease Disorders of Intracellular Cobalamin Metabolism
Variation info
Gene MTR
CLNDBN Disorders of Intracellular Cobalamin Metabolism
Reversed 0
HGVS NC_000001.10:g.237062432T>C
CLNSRC
CLNACC RCV000331743.1,