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rs4846051

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
(G;G) 0 common in clinvar
Make rs4846051(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position11794400
GeneMTHFR
is asnp
is mentioned by
dbSNPrs4846051
ebirs4846051
HLIrs4846051
Exacrs4846051
Varsomers4846051
Maprs4846051
PheGenIrs4846051
hapmaprs4846051
1000 genomesrs4846051
hgdprs4846051
ensemblrs4846051
gopubmedrs4846051
geneviewrs4846051
scholarrs4846051
googlers4846051
pharmgkbrs4846051
gwascentralrs4846051
openSNPrs4846051
23andMers4846051
23andMe allrs4846051
SNP Nexus

SNPshotrs4846051
SNPdbers4846051
MSV3drs4846051
GWAS Ctlgrs4846051
GMAF0.07438
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 18483346] Direct genotyping of single nucleotide polymorphisms in methyl metabolism genes using probe-free high-resolution melting analysis.


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


ClinVar
Risk rs4846051(A;A)
Alt rs4846051(A;A)
Reference rs4846051(G;G)
Significance Non-pathogenic
Disease not specified
Variation info
Gene MTHFR
CLNDBN not specified
Reversed 0
HGVS NC_000001.10:g.11854457G>A
CLNSRC
CLNACC RCV000153514.3,