rs3737967
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs3737967(C;T) |
Make rs3737967(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 1 |
Position | 11787392 |
Gene | C1orf167, MTHFR |
is a | snp |
is | mentioned by |
dbSNP | rs3737967 |
dbSNP (classic) | rs3737967 |
ClinGen | rs3737967 |
ebi | rs3737967 |
HLI | rs3737967 |
Exac | rs3737967 |
Gnomad | rs3737967 |
Varsome | rs3737967 |
LitVar | rs3737967 |
Map | rs3737967 |
PheGenI | rs3737967 |
Biobank | rs3737967 |
1000 genomes | rs3737967 |
hgdp | rs3737967 |
ensembl | rs3737967 |
geneview | rs3737967 |
scholar | rs3737967 |
rs3737967 | |
pharmgkb | rs3737967 |
gwascentral | rs3737967 |
openSNP | rs3737967 |
23andMe | rs3737967 |
SNPshot | rs3737967 |
SNPdbe | rs3737967 |
MSV3d | rs3737967 |
GWAS Ctlg | rs3737967 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 26689687] 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, |