rs868014
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs868014(C;C) |
Make rs868014(C;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 1 |
Position | 11789390 |
Gene | C1orf167, MTHFR |
is a | snp |
is | mentioned by |
dbSNP | rs868014 |
dbSNP (classic) | rs868014 |
ClinGen | rs868014 |
ebi | rs868014 |
HLI | rs868014 |
Exac | rs868014 |
Gnomad | rs868014 |
Varsome | rs868014 |
LitVar | rs868014 |
Map | rs868014 |
PheGenI | rs868014 |
Biobank | rs868014 |
1000 genomes | rs868014 |
hgdp | rs868014 |
ensembl | rs868014 |
geneview | rs868014 |
scholar | rs868014 |
rs868014 | |
pharmgkb | rs868014 |
gwascentral | rs868014 |
openSNP | rs868014 |
23andMe | rs868014 |
SNPshot | rs868014 |
SNPdbe | rs868014 |
MSV3d | rs868014 |
GWAS Ctlg | rs868014 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 28171870] Methylene Tetrahydrofolate Reductase (MTHFR) rs868014 Polymorphism Regulated by miR-1203 Associates with Risk and Short Term Outcome of Ischemic Stroke.
ClinVar | |
---|---|
Risk | rs868014(C;C) |
Alt | rs868014(C;C) |
Reference | Rs868014(T;T) |
Significance | Non-pathogenic |
Disease | Neural tube defects |
Variation | info |
Gene | MTHFR C1orf167 |
CLNDBN | Neural tube defects, folate-sensitive |
Reversed | 1 |
HGVS | NC_000001.10:g.11849447A>G |
CLNSRC | |
CLNACC | RCV000277799.1, |