rs26949
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs26949(A;A) |
Make rs26949(A;G) |
Make rs26949(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 5 |
Position | 60529473 |
Gene | PART1 |
is a | snp |
is | mentioned by |
dbSNP | rs26949 |
dbSNP (classic) | rs26949 |
ClinGen | rs26949 |
ebi | rs26949 |
HLI | rs26949 |
Exac | rs26949 |
Gnomad | rs26949 |
Varsome | rs26949 |
LitVar | rs26949 |
Map | rs26949 |
PheGenI | rs26949 |
Biobank | rs26949 |
1000 genomes | rs26949 |
hgdp | rs26949 |
ensembl | rs26949 |
geneview | rs26949 |
scholar | rs26949 |
rs26949 | |
pharmgkb | rs26949 |
gwascentral | rs26949 |
openSNP | rs26949 |
23andMe | rs26949 |
SNPshot | rs26949 |
SNPdbe | rs26949 |
MSV3d | rs26949 |
GWAS Ctlg | rs26949 |
GMAF | 0.3861 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 23360675] A genetic association study of NLRP2 and NLRP7 genes in idiopathic recurrent miscarriage
[PMID 16835261] Phosphodiesterase 4D polymorphisms and the risk of cerebral infarction in a biracial population: the Stroke Prevention in Young Women Study.
[PMID 19409523] Multilocus Bayesian meta-analysis of gene-disease associations.