Have questions? Visit https://www.reddit.com/r/SNPedia

rs3737967

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs3737967(C;T)
Make rs3737967(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position11787392
GeneC1orf167, MTHFR
is asnp
is mentioned by
dbSNPrs3737967
dbSNP (old)rs3737967
ClinGenrs3737967
ebirs3737967
HLIrs3737967
Exacrs3737967
Gnomadrs3737967
Varsomers3737967
Maprs3737967
PheGenIrs3737967
Biobankrs3737967
1000 genomesrs3737967
hgdprs3737967
ensemblrs3737967
gopubmedrs3737967
geneviewrs3737967
scholarrs3737967
googlers3737967
pharmgkbrs3737967
gwascentralrs3737967
openSNPrs3737967
23andMers3737967
23andMe allrs3737967
SNP Nexus

SNPshotrs3737967
SNPdbers3737967
MSV3drs3737967
GWAS Ctlgrs3737967
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 26689687OA-icon.png] Associations of Polymorphisms in MTHFR Gene with the Risk of Age-Related Cataract in Chinese Han Population: A Genotype-Phenotype Analysis.


ClinVar
Risk rs3737967(T;T)
Alt rs3737967(T;T)
Reference Rs3737967(C;C)
Significance Probable-non-pathogenic
Disease Neural tube defects
Variation info
Gene MTHFR C1orf167
CLNDBN Neural tube defects, folate-sensitive
Reversed 1
HGVS NC_000001.10:g.11847449G>A
CLNSRC
CLNACC RCV000318902.1,