rs17231520
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs17231520(A;A) |
Make rs17231520(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 56961915 |
Gene | CETP |
is a | snp |
is | mentioned by |
dbSNP | rs17231520 |
dbSNP (classic) | rs17231520 |
ClinGen | rs17231520 |
ebi | rs17231520 |
HLI | rs17231520 |
Exac | rs17231520 |
Gnomad | rs17231520 |
Varsome | rs17231520 |
LitVar | rs17231520 |
Map | rs17231520 |
PheGenI | rs17231520 |
Biobank | rs17231520 |
1000 genomes | rs17231520 |
hgdp | rs17231520 |
ensembl | rs17231520 |
geneview | rs17231520 |
scholar | rs17231520 |
rs17231520 | |
pharmgkb | rs17231520 |
gwascentral | rs17231520 |
openSNP | rs17231520 |
23andMe | rs17231520 |
SNPshot | rs17231520 |
SNPdbe | rs17231520 |
MSV3d | rs17231520 |
GWAS Ctlg | rs17231520 |
GMAF | 0.01837 |
Max Magnitude | 0 |
[PMID 22539988] Evaluation of the Metabochip Genotyping Array in African Americans and Implications for Fine Mapping of GWAS-Identified Loci: The PAGE Study
ClinVar | |
---|---|
Risk | rs17231520(A;A) |
Alt | rs17231520(A;A) |
Reference | Rs17231520(G;G) |
Significance | Non-pathogenic |
Disease | Hyperalphalipoproteinemia |
Variation | info |
Gene | CETP |
CLNDBN | Hyperalphalipoproteinemia |
Reversed | 0 |
HGVS | NC_000016.9:g.56995827G>A |
CLNSRC | |
CLNACC | RCV000378884.1, |