rs464218
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs464218(C;C) |
Make rs464218(C;T) |
Make rs464218(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 1 |
Position | 109313684 |
Gene | SORT1 |
is a | snp |
is | mentioned by |
dbSNP | rs464218 |
dbSNP (classic) | rs464218 |
ClinGen | rs464218 |
ebi | rs464218 |
HLI | rs464218 |
Exac | rs464218 |
Gnomad | rs464218 |
Varsome | rs464218 |
LitVar | rs464218 |
Map | rs464218 |
PheGenI | rs464218 |
Biobank | rs464218 |
1000 genomes | rs464218 |
hgdp | rs464218 |
ensembl | rs464218 |
geneview | rs464218 |
scholar | rs464218 |
rs464218 | |
pharmgkb | rs464218 |
gwascentral | rs464218 |
openSNP | rs464218 |
23andMe | rs464218 |
SNPshot | rs464218 |
SNPdbe | rs464218 |
MSV3d | rs464218 |
GWAS Ctlg | rs464218 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 26464717] Association of variants in CELSR2-PSRC1-SORT1 with risk of serum lipid traits, coronary artery disease and ischemic stroke