rs189798
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 2 | normal high myopia risk |
(C;T) | 2 | decreased high myopia risk |
(T;T) | 2.1 | decreased high myopia risk |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 9133067 |
is a | snp |
is | mentioned by |
dbSNP | rs189798 |
dbSNP (classic) | rs189798 |
ClinGen | rs189798 |
ebi | rs189798 |
HLI | rs189798 |
Exac | rs189798 |
Gnomad | rs189798 |
Varsome | rs189798 |
LitVar | rs189798 |
Map | rs189798 |
PheGenI | rs189798 |
Biobank | rs189798 |
1000 genomes | rs189798 |
hgdp | rs189798 |
ensembl | rs189798 |
geneview | rs189798 |
scholar | rs189798 |
rs189798 | |
pharmgkb | rs189798 |
gwascentral | rs189798 |
openSNP | rs189798 |
23andMe | rs189798 |
SNPshot | rs189798 |
SNPdbe | rs189798 |
MSV3d | rs189798 |
GWAS Ctlg | rs189798 |
GMAF | 0.3815 |
Max Magnitude | 2.1 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 23049088] A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French population
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 8
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d