rs289747
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs289747(A;A) |
Make rs289747(A;G) |
Make rs289747(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 56990026 |
Gene | NLRC5 |
is a | snp |
is | mentioned by |
dbSNP | rs289747 |
dbSNP (classic) | rs289747 |
ClinGen | rs289747 |
ebi | rs289747 |
HLI | rs289747 |
Exac | rs289747 |
Gnomad | rs289747 |
Varsome | rs289747 |
LitVar | rs289747 |
Map | rs289747 |
PheGenI | rs289747 |
Biobank | rs289747 |
1000 genomes | rs289747 |
hgdp | rs289747 |
ensembl | rs289747 |
geneview | rs289747 |
scholar | rs289747 |
rs289747 | |
pharmgkb | rs289747 |
gwascentral | rs289747 |
openSNP | rs289747 |
23andMe | rs289747 |
SNPshot | rs289747 |
SNPdbe | rs289747 |
MSV3d | rs289747 |
GWAS Ctlg | rs289747 |
GMAF | 0.3448 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 21859556] Association Study of Selected Genetic Polymorphisms and Occurrence of Venous Thromboembolism in Patients With Multiple Myeloma Who Were Treated With Thalidomide
[PMID 18787502] Genetic contributions to the development of retinopathy of prematurity.
[PMID 19682379] TagSNP transferability and relative loss of variability prediction from HapMap to an admixed population.