rs1780316
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs1780316(C;C) |
Make rs1780316(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 21563142 |
Gene | ALPL |
is a | snp |
is | mentioned by |
dbSNP | rs1780316 |
dbSNP (classic) | rs1780316 |
ClinGen | rs1780316 |
ebi | rs1780316 |
HLI | rs1780316 |
Exac | rs1780316 |
Gnomad | rs1780316 |
Varsome | rs1780316 |
LitVar | rs1780316 |
Map | rs1780316 |
PheGenI | rs1780316 |
Biobank | rs1780316 |
1000 genomes | rs1780316 |
hgdp | rs1780316 |
ensembl | rs1780316 |
geneview | rs1780316 |
scholar | rs1780316 |
rs1780316 | |
pharmgkb | rs1780316 |
gwascentral | rs1780316 |
openSNP | rs1780316 |
23andMe | rs1780316 |
SNPshot | rs1780316 |
SNPdbe | rs1780316 |
MSV3d | rs1780316 |
GWAS Ctlg | rs1780316 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 25147783] Genetic Associations with Plasma B12, B6, and Folate Levels in an Ischemic Stroke Population from the Vitamin Intervention for Stroke Prevention (VISP) Trial
ClinVar | |
---|---|
Risk | rs1780316(C;C) |
Alt | rs1780316(C;C) |
Reference | Rs1780316(T;T) |
Significance | Non-pathogenic |
Disease | not specified |
Variation | info |
Gene | ALPL |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000001.10:g.21889635T>C |
CLNSRC | |
CLNACC | RCV000178778.1, |