rs788016
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;G) | 0 |
Make rs788016(A;A) |
Make rs788016(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 197487569 |
Gene | HSPD1, SNORA105B |
is a | snp |
is | mentioned by |
dbSNP | rs788016 |
dbSNP (classic) | rs788016 |
ClinGen | rs788016 |
ebi | rs788016 |
HLI | rs788016 |
Exac | rs788016 |
Gnomad | rs788016 |
Varsome | rs788016 |
LitVar | rs788016 |
Map | rs788016 |
PheGenI | rs788016 |
Biobank | rs788016 |
1000 genomes | rs788016 |
hgdp | rs788016 |
ensembl | rs788016 |
geneview | rs788016 |
scholar | rs788016 |
rs788016 | |
pharmgkb | rs788016 |
gwascentral | rs788016 |
openSNP | rs788016 |
23andMe | rs788016 |
SNPshot | rs788016 |
SNPdbe | rs788016 |
MSV3d | rs788016 |
GWAS Ctlg | rs788016 |
GMAF | 0.3871 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 18320357] G-C-T-C haplotype of rs2340690-rs788016-rs2305560-rs2565163 has odds ratio of 1.91 (CI: 1.26-2.89, p=0.002) for coronary heart disease compared to G-T-T-C, based on a study of 1,000 Han Chinese patients and matched controls.
- Note: Haplotype allele assignments may not be in dbSNP orientation.