rs6668352
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6668352(A;A) |
Make rs6668352(A;G) |
Make rs6668352(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 11854772 |
is a | snp |
is | mentioned by |
dbSNP | rs6668352 |
dbSNP (classic) | rs6668352 |
ClinGen | rs6668352 |
ebi | rs6668352 |
HLI | rs6668352 |
Exac | rs6668352 |
Gnomad | rs6668352 |
Varsome | rs6668352 |
LitVar | rs6668352 |
Map | rs6668352 |
PheGenI | rs6668352 |
Biobank | rs6668352 |
1000 genomes | rs6668352 |
hgdp | rs6668352 |
ensembl | rs6668352 |
geneview | rs6668352 |
scholar | rs6668352 |
rs6668352 | |
pharmgkb | rs6668352 |
gwascentral | rs6668352 |
openSNP | rs6668352 |
23andMe | rs6668352 |
SNPshot | rs6668352 |
SNPdbe | rs6668352 |
MSV3d | rs6668352 |
GWAS Ctlg | rs6668352 |
GMAF | 0.1965 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
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[PMID 19326473] Natriuretic peptide system gene variants are associated with ventricular dysfunction after coronary artery bypass grafting.
[PMID 21273288] Genome-wide association analysis and fine mapping of NT-proBNP level provide novel insight into the role of the MTHFR-CLCN6-NPPA-NPPB gene cluster.