rs980238
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs980238(A;A) |
Make rs980238(A;C) |
Make rs980238(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 4425096 |
Gene | CSMD1 |
is a | snp |
is | mentioned by |
dbSNP | rs980238 |
dbSNP (classic) | rs980238 |
ClinGen | rs980238 |
ebi | rs980238 |
HLI | rs980238 |
Exac | rs980238 |
Gnomad | rs980238 |
Varsome | rs980238 |
LitVar | rs980238 |
Map | rs980238 |
PheGenI | rs980238 |
Biobank | rs980238 |
1000 genomes | rs980238 |
hgdp | rs980238 |
ensembl | rs980238 |
geneview | rs980238 |
scholar | rs980238 |
rs980238 | |
pharmgkb | rs980238 |
gwascentral | rs980238 |
openSNP | rs980238 |
23andMe | rs980238 |
SNPshot | rs980238 |
SNPdbe | rs980238 |
MSV3d | rs980238 |
GWAS Ctlg | rs980238 |
GMAF | 0.3728 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 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 | A |
P-val | 9E-6 |
Odds Ratio | .10 [0.055-0.145] unit decrease |