rs11860115
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11860115(A;A) |
Make rs11860115(A;C) |
Make rs11860115(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 67943793 |
Gene | LCAT, SLC12A4 |
is a | snp |
is | mentioned by |
dbSNP | rs11860115 |
dbSNP (classic) | rs11860115 |
ClinGen | rs11860115 |
ebi | rs11860115 |
HLI | rs11860115 |
Exac | rs11860115 |
Gnomad | rs11860115 |
Varsome | rs11860115 |
LitVar | rs11860115 |
Map | rs11860115 |
PheGenI | rs11860115 |
Biobank | rs11860115 |
1000 genomes | rs11860115 |
hgdp | rs11860115 |
ensembl | rs11860115 |
geneview | rs11860115 |
scholar | rs11860115 |
rs11860115 | |
pharmgkb | rs11860115 |
gwascentral | rs11860115 |
openSNP | rs11860115 |
23andMe | rs11860115 |
SNPshot | rs11860115 |
SNPdbe | rs11860115 |
MSV3d | rs11860115 |
GWAS Ctlg | rs11860115 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 24789697] Identification of genetic variants of lecithin cholesterol acyltransferase in individuals with high HDL‑C levels