rs6617
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6617(C;C) |
Make rs6617(C;G) |
Make rs6617(G;G) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 3 |
Position | 52706166 |
Gene | GLT8D1, SPCS1 |
is a | snp |
is | mentioned by |
dbSNP | rs6617 |
dbSNP (classic) | rs6617 |
ClinGen | rs6617 |
ebi | rs6617 |
HLI | rs6617 |
Exac | rs6617 |
Gnomad | rs6617 |
Varsome | rs6617 |
LitVar | rs6617 |
Map | rs6617 |
PheGenI | rs6617 |
Biobank | rs6617 |
1000 genomes | rs6617 |
hgdp | rs6617 |
ensembl | rs6617 |
geneview | rs6617 |
scholar | rs6617 |
rs6617 | |
pharmgkb | rs6617 |
gwascentral | rs6617 |
openSNP | rs6617 |
23andMe | rs6617 |
SNPshot | rs6617 |
SNPdbe | rs6617 |
MSV3d | rs6617 |
GWAS Ctlg | rs6617 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
[PMID 29942097] Common variants in the GNL3 contribute to the increasing risk of knee osteoarthritis in Han Chinese population.