rs11754641
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common genotype |
Make rs11754641(C;G) |
Make rs11754641(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 64926030 |
Gene | EYS |
is a | snp |
is | mentioned by |
dbSNP | rs11754641 |
dbSNP (classic) | rs11754641 |
ClinGen | rs11754641 |
ebi | rs11754641 |
HLI | rs11754641 |
Exac | rs11754641 |
Gnomad | rs11754641 |
Varsome | rs11754641 |
LitVar | rs11754641 |
Map | rs11754641 |
PheGenI | rs11754641 |
Biobank | rs11754641 |
1000 genomes | rs11754641 |
hgdp | rs11754641 |
ensembl | rs11754641 |
geneview | rs11754641 |
scholar | rs11754641 |
rs11754641 | |
pharmgkb | rs11754641 |
gwascentral | rs11754641 |
openSNP | rs11754641 |
23andMe | rs11754641 |
SNPshot | rs11754641 |
SNPdbe | rs11754641 |
MSV3d | rs11754641 |
GWAS Ctlg | rs11754641 |
GMAF | 0.04821 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22993228] |
Trait | Disc degeneration (lumbar) |
Title | Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects. |
Risk Allele | C |
P-val | 8E-6 |
Odds Ratio | .29 [0.16-0.42] unit increase |