rs6698843
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6698843(C;C) |
Make rs6698843(C;T) |
Make rs6698843(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 1 |
Position | 109264212 |
Gene | CELSR2 |
is a | snp |
is | mentioned by |
dbSNP | rs6698843 |
dbSNP (classic) | rs6698843 |
ClinGen | rs6698843 |
ebi | rs6698843 |
HLI | rs6698843 |
Exac | rs6698843 |
Gnomad | rs6698843 |
Varsome | rs6698843 |
LitVar | rs6698843 |
Map | rs6698843 |
PheGenI | rs6698843 |
Biobank | rs6698843 |
1000 genomes | rs6698843 |
hgdp | rs6698843 |
ensembl | rs6698843 |
geneview | rs6698843 |
scholar | rs6698843 |
rs6698843 | |
pharmgkb | rs6698843 |
gwascentral | rs6698843 |
openSNP | rs6698843 |
23andMe | rs6698843 |
SNPshot | rs6698843 |
SNPdbe | rs6698843 |
MSV3d | rs6698843 |
GWAS Ctlg | rs6698843 |
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