rs16982743
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs16982743(A;A) |
Make rs16982743(A;G) |
Make rs16982743(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 51501649 |
Gene | SIGLEC12 |
is a | snp |
is | mentioned by |
dbSNP | rs16982743 |
dbSNP (classic) | rs16982743 |
ClinGen | rs16982743 |
ebi | rs16982743 |
HLI | rs16982743 |
Exac | rs16982743 |
Gnomad | rs16982743 |
Varsome | rs16982743 |
LitVar | rs16982743 |
Map | rs16982743 |
PheGenI | rs16982743 |
Biobank | rs16982743 |
1000 genomes | rs16982743 |
hgdp | rs16982743 |
ensembl | rs16982743 |
geneview | rs16982743 |
scholar | rs16982743 |
rs16982743 | |
pharmgkb | rs16982743 |
gwascentral | rs16982743 |
openSNP | rs16982743 |
23andMe | rs16982743 |
SNPshot | rs16982743 |
SNPdbe | rs16982743 |
MSV3d | rs16982743 |
GWAS Ctlg | rs16982743 |
GMAF | 0.1873 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 23690342] Pharmacogenomic Association of Nonsynonymous SNPs in SIGLEC12, A1BG, and the Selectin Region and Cardiovascular Outcomes
[PMID 19200524] A genome-wide survey of the prevalence and evolutionary forces acting on human nonsense SNPs.