rs12038826
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common genotype |
Make rs12038826(C;C) |
Make rs12038826(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 230787205 |
Gene | CAPN9, LOC107985359 |
is a | snp |
is | mentioned by |
dbSNP | rs12038826 |
dbSNP (classic) | rs12038826 |
ClinGen | rs12038826 |
ebi | rs12038826 |
HLI | rs12038826 |
Exac | rs12038826 |
Gnomad | rs12038826 |
Varsome | rs12038826 |
LitVar | rs12038826 |
Map | rs12038826 |
PheGenI | rs12038826 |
Biobank | rs12038826 |
1000 genomes | rs12038826 |
hgdp | rs12038826 |
ensembl | rs12038826 |
geneview | rs12038826 |
scholar | rs12038826 |
rs12038826 | |
pharmgkb | rs12038826 |
gwascentral | rs12038826 |
openSNP | rs12038826 |
23andMe | rs12038826 |
SNPshot | rs12038826 |
SNPdbe | rs12038826 |
MSV3d | rs12038826 |
GWAS Ctlg | rs12038826 |
GMAF | 0.06749 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23049088] |
Trait | Myopia (pathological) |
Title | A Genome-Wide Association Study Provides Evidence for Association of Chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with High Myopia in the French Population. |
Risk Allele | |
P-val | 7E-6 |
Odds Ratio | NR NR |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 1
- 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