rs6748795
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6748795(C;C) |
Make rs6748795(C;G) |
Make rs6748795(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 223986006 |
Gene | SERPINE2 |
is a | snp |
is | mentioned by |
dbSNP | rs6748795 |
dbSNP (classic) | rs6748795 |
ClinGen | rs6748795 |
ebi | rs6748795 |
HLI | rs6748795 |
Exac | rs6748795 |
Gnomad | rs6748795 |
Varsome | rs6748795 |
LitVar | rs6748795 |
Map | rs6748795 |
PheGenI | rs6748795 |
Biobank | rs6748795 |
1000 genomes | rs6748795 |
hgdp | rs6748795 |
ensembl | rs6748795 |
geneview | rs6748795 |
scholar | rs6748795 |
rs6748795 | |
pharmgkb | rs6748795 |
gwascentral | rs6748795 |
openSNP | rs6748795 |
23andMe | rs6748795 |
SNPshot | rs6748795 |
SNPdbe | rs6748795 |
MSV3d | rs6748795 |
GWAS Ctlg | rs6748795 |
GMAF | 0.4545 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
[PMID 22145704] SERPINE2 haplotype as a risk factor for panlobular type of emphysema
[PMID 19949669] SERPINE2 polymorphisms and chronic obstructive pulmonary disease.