rs16830359
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs16830359(A;A) |
Make rs16830359(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 43130713 |
is a | snp |
is | mentioned by |
dbSNP | rs16830359 |
dbSNP (classic) | rs16830359 |
ClinGen | rs16830359 |
ebi | rs16830359 |
HLI | rs16830359 |
Exac | rs16830359 |
Gnomad | rs16830359 |
Varsome | rs16830359 |
LitVar | rs16830359 |
Map | rs16830359 |
PheGenI | rs16830359 |
Biobank | rs16830359 |
1000 genomes | rs16830359 |
hgdp | rs16830359 |
ensembl | rs16830359 |
geneview | rs16830359 |
scholar | rs16830359 |
rs16830359 | |
pharmgkb | rs16830359 |
gwascentral | rs16830359 |
openSNP | rs16830359 |
23andMe | rs16830359 |
SNPshot | rs16830359 |
SNPdbe | rs16830359 |
MSV3d | rs16830359 |
GWAS Ctlg | rs16830359 |
GMAF | 0.05051 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21348951] |
Trait | |
Title | Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality |
Risk Allele | |
P-val | 1E-7 |
Odds Ratio | None None |